DISPOSABLE SLIDE VALVE MANIFOLD
FDA 510(k) clearance K913094 · decided 1992-01-27
Clearance details
- K-number
- K913094
- Device name
- DISPOSABLE SLIDE VALVE MANIFOLD
- Applicant
- Professional Medical Services
- Decision
- Substantially Equivalent
- Date received
- 1991-07-12
- Decision date
- 1992-01-27
- Days to decision
- 199 days
- Clearance type
- Traditional
- Product code
- DQO
- Device class
- 2
- Regulation number
- 870.1200
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- North Salt Lake, UT, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.