510(k) clearances

PacePro Wire

Opsens, Inc. · Cardiovascular

K240864Substantially EquivalentTraditionalDQX
Open FDA's page for this record
Third party flag
N
City
Quebec
Advisory committee description
Cardiovascular
Address 1
750 Blvd. Du Parc Technologique
Statement or summary
Summary
Product code
DQX
Zip code
G1P 4S3
Applicant
Opsens, Inc.
Decision date
2024-05-24
Decision code
SESE
Country code
CA
Device name
PacePro Wire
Advisory committee
CV
Contact
Marc Chaunet
K number
K240864
Date received
2024-03-28
Review advisory committee
CV
Postal code
G1P 4S3
Decision description
Substantially Equivalent
Clearance type
Traditional
Harmonized identifiers (openFDA)
Device name
Wire, Guide, Catheter
Medical specialty description
Cardiovascular
Regulation number
870.1330
Device class
2
Registration number
3013656790, 3009600098, 3030446844, 3000268902, 9616088, 3014716786, 2953200, 1313046, 3020954746, 3009018440, 3012159165, 2527072, 3006010712, 3008837339, 3003768277, 1000523114, 9612812, 3030452144, 3007695959, 3006946276, 9617592, 3007138831, 1061124, 1055236, 3006425876, 2134285, 1226348, 2017865, 3005334138, 2134812, 2024168, 3009957947, 3042175841, 3008114965, 3009756153, 3004111573, 3033589330, 3011137372, 3013764800, 2246552 +221 more
FEI number
3013656790, 3009600098, 3030446844, 3000268902, 3014716786, 1313046, 2828, 3002806565, 3009018440, 3012159165, 3020954746, 3006010712, 2527072, 3008837339, 1000523114, 3030452144, 3007695959, 1000120555, 3006946276, 3007138831, 3006425876, 2017865, 3005334138, 2024168, 3009957947, 3042175841, 3008114965, 3009756153, 3004111573, 3033589330, 3000206435, 3001236905, 3013764800, 2246552, 3001124136, 3018784828, 3030574705, 3012497308, 3002913962, 3002917664 +220 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.