KEY VASCULAR BOOTIES
FDA 510(k) clearance K896472 · decided 1989-12-14
Clearance details
- K-number
- K896472
- Device name
- KEY VASCULAR BOOTIES
- Applicant
- Key Surgical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1989-11-13
- Decision date
- 1989-12-14
- Days to decision
- 31 days
- Clearance type
- Traditional
- Product code
- MAW
- Device class
- 1
- Regulation number
- 878.4800
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Minneapolis, MN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.