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PROVOX HME CASSETTE - Provox Hme Cassette, Model 7240
FDA 510(k)Class II (US FDA 510(k))
510(k) K014102
Identifiers
- 510(k) Number
- K014102 FDA 510(k)
- FDA Product Code
- JOH FDA 510(k)
- Models / Variants
- Provox Hme Cassette, Model 7240 FDA 510(k)Provox Adhesive, Model 7251 FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 868.5800 FDA 510(k)
- Regulation Number
- 868.5800 FDA 510(k)
- Advisory Committee
- Anesthesiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
PROVOX HME CASSETTE - Provox Hme Cassette, Model 7240 by Atos Medical AB — Class II — FDA_510K — listed in FDA 510(k) — 2 models — 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 | K014102 | Class II | Active |
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Manufacturer
- Manufacturer
- Atos Medical AB
Sources (1)
- FDA 510(k) K014102 24 fields · synced Jun 18, 2026