4MM CUP CURRETTE
FDA 510(k) clearance K841979 · decided 1984-06-19
Clearance details
- K-number
- K841979
- Device name
- 4MM CUP CURRETTE
- Applicant
- Stainless Mfg., Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-05-14
- Decision date
- 1984-06-19
- Days to decision
- 36 days
- Clearance type
- Traditional
- Product code
- HTF
- Device class
- 1
- Regulation number
- 878.4800
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| BONE CURETTE (K890252) | Kinetic Medical Products | 1989-01-27 |
| ACROMED WALLIE-HEINIG CURETTES (K870778) | Buckman Co., Inc. | 1987-03-09 |
Recalls involving this device
No recalls on record reference this clearance.