Identity
- Trade Name
- EnSite™ Velocity™ FDA UDI
- Generic Name
- Cardiac mapping system application software FDA UDI
- Device Name
- Utility Upgrade Kit FDA UDI
- Model / Reference
- H702323 FDA UDI
- Description
- Utility Upgrade Kit FDA UDI
Identifiers
- Catalog Number
- H702323 FDA UDI
- Primary DI / UDI-DI
- 05415067023230 FDA UDI
- 510(k) Number
- K201181 FDA UDI
- FDA Product Code
- DQK FDA UDI
- GMDN Term
- Cardiac mapping system application software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1425 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Cardiac mapping system application software
EnSite™ Velocity™ by St. Jude Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Cardiac mapping system application software.
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- STAR Apollo — RHYTHM AI INC · Class II
- EchoGo — Ultromics, Ltd. · Class II
Cleared under the same submission
K201181 also covers:
- Advisor™ — ST. JUDE MEDICAL, INC.
- Advisor™ FL Mapping Catheter, Sensor Enabled™ — ST. JUDE MEDICAL, INC.
- Advisor™ HD Grid Mapping Catheter — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- St. Jude Medical, Inc.
Sources (1)
- FDA UDI 88473f97-32ae-4d2c-a79a-f6e6e24dfed5 36 fields · synced May 30, 2026