The following data is part of a premarket notification filed by Helena Laboratories with the FDA for Rep Hemoglobin Ief Kits (cat. No. 3250).
| Device ID | K901143 |
| 510k Number | K901143 |
| Device Name: | REP HEMOGLOBIN IEF KITS (CAT. NO. 3250) |
| Classification | System, Analysis, Electrophoretic Hemoglobin |
| Applicant | HELENA LABORATORIES 1530 LINDBERGH DR. P.O. BOX 752 Beaumont, TX 77704 |
| Contact | Pat Franks |
| Correspondent | Pat Franks HELENA LABORATORIES 1530 LINDBERGH DR. P.O. BOX 752 Beaumont, TX 77704 |
| Product Code | JBD |
| CFR Regulation Number | 864.7440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-03-12 |
| Decision Date | 1990-05-23 |