The following data is part of a premarket notification filed by Hybritech, Inc. with the FDA for Tandem(r) M-pak(tm) Total B-hcg Immunoenzy. Assay.
| Device ID | K870521 |
| 510k Number | K870521 |
| Device Name: | TANDEM(R) M-PAK(TM) TOTAL B-HCG IMMUNOENZY. ASSAY |
| Classification | Visual, Pregnancy Hcg, Prescription Use |
| Applicant | HYBRITECH, INC. 11095 TORREYANA RD. P.O. BOX 269006 San Diego, CA 92126 |
| Contact | Kabakoff, Phd |
| Correspondent | Kabakoff, Phd HYBRITECH, INC. 11095 TORREYANA RD. P.O. BOX 269006 San Diego, CA 92126 |
| Product Code | JHI |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-02-06 |
| Decision Date | 1987-04-08 |