CPI PRINTER
FDA 510(k) clearance K822857 · decided 1983-01-08
Clearance details
- K-number
- K822857
- Device name
- CPI PRINTER
- Applicant
- Cardiac Pacemakers, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-09-27
- Decision date
- 1983-01-08
- Days to decision
- 103 days
- Clearance type
- Traditional
- Product code
- KAG
- Device class
- 1
- Regulation number
- 878.1800
- 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 |
|---|---|---|
| DRABKIN REAGENT (K842931) | E K Ind., Inc. | 1984-09-21 |
Recalls involving this device
No recalls on record reference this clearance.