HEMOSTAT
FDA 510(k) clearance K770158 · decided 1977-01-31
Clearance details
- K-number
- K770158
- Device name
- HEMOSTAT
- Applicant
- Deringer-Ney, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1977-01-24
- Decision date
- 1977-01-31
- Days to decision
- 7 days
- Clearance type
- Traditional
- Product code
- EMD
- 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 |
|---|---|---|
| HEMOSTAT, SURGICAL (VARIOUS TYPES) (K920883) | S.T.S Instruments | 1992-03-13 |
Recalls involving this device
No recalls on record reference this clearance.