← Back to catalogue
Defibrillator Analyzer - Da-2006p
FDA 510(k)Class II (US FDA 510(k))
510(k) K110192
Identifiers
- 510(k) Number
- K110192 FDA 510(k)
- FDA Product Code
- DRL FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.5325 FDA 510(k)
- Regulation Number
- 870.5325 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Defibrillator Analyzer - Da-2006p by Bc Group International, Inc. — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
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 | K110192 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bc Group International, Inc.
Sources (1)
- FDA 510(k) K110192 24 fields · synced Jun 18, 2026