FEMORAL ARTERY PRESSURE PAD/DISK
FDA 510(k) clearance K914149 · decided 1991-12-13
Clearance details
- K-number
- K914149
- Device name
- FEMORAL ARTERY PRESSURE PAD/DISK
- Applicant
- Disco, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-09-16
- Decision date
- 1991-12-13
- Days to decision
- 88 days
- Clearance type
- Traditional
- Product code
- DXC
- Device class
- 2
- Regulation number
- 870.4450
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Portland, OR, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.