SMARTRECORDER, MODEL 2500— 510(k) K990199
Substantially EquivalentRespironics, Inc.
FDA 510(k) clearance K990199 for SMARTRECORDER, MODEL 2500, Substantially Equivalent on 1999-04-19. Applicant: Respironics, Inc.. Device class: 2.
Clearance details
- Applicant
- Respironics, Inc.
- Product code
- Code MNR
- Device class
- Class 2
- Regulation
- 21 CFR 868.2375
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pittsburgh, PA, US
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