SCISSORS SHEA BELLUCC
FDA 510(k) clearance K833603 · decided 1984-01-03
Clearance details
- K-number
- K833603
- Device name
- SCISSORS SHEA BELLUCC
- Applicant
- Microtek Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1983-10-12
- Decision date
- 1984-01-03
- Days to decision
- 83 days
- Clearance type
- Traditional
- Product code
- JZB
- Device class
- 1
- Regulation number
- 874.4420
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- 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 |
|---|---|---|
| ACA(R) BETA-2-MICROGLOBULIN (B2M) TEST PACK (K914226) | E.I. Dupont DE Nemours & Co., Inc. | 1991-11-19 |
| VEIN GRAFT EAR SCISSORS (K870756) | Treace Medical, Inc. | 1987-03-03 |
| EAR SCISSORS (K822196) | Kelleher Corp. | 1982-08-30 |
Recalls involving this device
No recalls on record reference this clearance.