VACU-AIDE
FDA 510(k) clearance K872094 · decided 1987-10-15
Clearance details
- K-number
- K872094
- Device name
- VACU-AIDE
- Applicant
- The Devilbiss Co.
- Decision
- Substantially Equivalent
- Date received
- 1987-06-01
- Decision date
- 1987-10-15
- Days to decision
- 136 days
- Clearance type
- Traditional
- Product code
- JCX
- Device class
- 2
- Regulation number
- 878.4780
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Somerset, PA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.