ALPINE V
FDA 510(k) clearance K914916 · decided 1992-09-23
Clearance details
- K-number
- K914916
- Device name
- ALPINE V
- Applicant
- Mountain Medical Equipment, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-11-04
- Decision date
- 1992-09-23
- Days to decision
- 324 days
- Clearance type
- Traditional
- Product code
- CAW
- Device class
- 2
- Regulation number
- 868.5440
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Littleton, CO, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.