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Padtak Pediatric Defib/Cardiovert/Pace/Monitor-Radiotransparent (2x2.25) (2602 …
FDA 510(k)Class II (US FDA 510(k))
510(k) K983232
Identifiers
- 510(k) Number
- K983232 FDA 510(k)
- FDA Product Code
- DRO FDA 510(k)
- Models / Variants
- 2602 FDA 510(k)Padtak Pediatric Defib FDA 510(k)Cardiovert FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.5550 FDA 510(k)
- Regulation Number
- 870.5550 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Padtak Pediatric Defib/Cardiovert/Pace/Monitor-Radiotransparent (2x2.25) (2602 … by Tz Medical, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 3 models
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K983232 | Class II | Active |
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Manufacturer
- Manufacturer
- Tz Medical, Inc.
Sources (1)
- FDA 510(k) K983232 24 fields · synced Oct 9, 2026