TONSIL SCISSORS 7
FDA 510(k) clearance K821292 · decided 1982-05-28
Clearance details
- K-number
- K821292
- Device name
- TONSIL SCISSORS 7
- Applicant
- Conphar, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-05-04
- Decision date
- 1982-05-28
- Days to decision
- 24 days
- Clearance type
- Traditional
- Product code
- EGN
- Device class
- 1
- Regulation number
- 872.4565
- Medical specialty
- Dental
- Advisory committee
- Dental
- 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 |
|---|---|---|
| GXP DENTAL X-RAY PROCESSOR (K932675) | Gendex Corp. | 1993-07-26 |
| 1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS (K851720) | Artiberia | 1985-07-02 |
| MAYO SCISSOR CURYED 5 1/2 (K821276) | Conphar, Inc. | 1982-05-28 |
| TONSIL SCISSORS STRAIGHT 5 1/2 (K821294) | Conphar, Inc. | 1982-05-28 |
| MAYO SCISSOR STRAIGHT 5 1/2 (K821275) | Conphar, Inc. | 1982-05-28 |
| CONPHAR (K821077) | Conphar, Inc. | 1982-05-24 |
Recalls involving this device
No recalls on record reference this clearance.