← Back to catalogue
Penlon I.d.p. Presssure Failure Alarm
FDA 510(k)Class II (US FDA 510(k))
510(k) K801254
by Penlon, Inc.
Identifiers
- 510(k) Number
- K801254 FDA 510(k)
- FDA Product Code
- CAP FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 868.2600 FDA 510(k)
- Regulation Number
- 868.2600 FDA 510(k)
- Advisory Committee
- Anesthesiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Penlon I.d.p. Presssure Failure Alarm by Penlon, 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 | K801254 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Penlon, Inc.
Sources (1)
- FDA 510(k) K801254 24 fields · synced Jun 18, 2026