COSGROVE CLAMP
FDA 510(k) clearance K974769 · decided 1998-06-12
Clearance details
- K-number
- K974769
- Device name
- COSGROVE CLAMP
- Applicant
- Allegiance Healthcare Corp.
- Decision
- Substantially Equivalent
- Date received
- 1997-12-22
- Decision date
- 1998-06-12
- Days to decision
- 172 days
- Clearance type
- Traditional
- Product code
- DXC
- Device class
- 2
- Regulation number
- 870.4450
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Mcgraw Park, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.