The following data is part of a premarket notification filed by Isolab, Inc. with the FDA for Hemocard Hemoglobin E.
| Device ID | K930070 |
| 510k Number | K930070 |
| Device Name: | HEMOCARD HEMOGLOBIN E |
| Classification | Nadh Oxidation/nad Reduction, Alt/sgpt |
| Applicant | ISOLAB, INC. DRAWER 4350 Akron, OH 44321 |
| Contact | Janet D Perkins |
| Correspondent | Janet D Perkins ISOLAB, INC. DRAWER 4350 Akron, OH 44321 |
| Product Code | CKA |
| CFR Regulation Number | 862.1030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-01-06 |
| Decision Date | 1993-04-08 |