16 GA X 6 BULLET POINT NEEDLE
FDA 510(k) clearance K894872 · decided 1989-09-22
Clearance details
- K-number
- K894872
- Device name
- 16 GA X 6 BULLET POINT NEEDLE
- Applicant
- R. J. Doyle, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1989-08-01
- Decision date
- 1989-09-22
- Days to decision
- 52 days
- Clearance type
- Traditional
- Product code
- GAA
- Device class
- 1
- Regulation number
- 878.4800
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Spirit Lake, ID, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.