RESPIRONICS' DIGITAL MANOMETER— 510(k) K904935
Substantially EquivalentRespironics, Inc.
FDA 510(k) clearance K904935 for RESPIRONICS' DIGITAL MANOMETER, Substantially Equivalent on 1991-04-03. Applicant: Respironics, Inc.. Device class: 2.
Clearance details
- Applicant
- Respironics, Inc.
- Product code
- Code CAP
- Device class
- Class 2
- Regulation
- 21 CFR 868.2600
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Murrysville, PA, US
Recent devices under product code CAP
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