The following data is part of a premarket notification filed by Difco Laboratories, Inc. with the FDA for Cellmatic Chlamydia Culture Confirm-difco-1000.
| Device ID | K860292 |
| 510k Number | K860292 |
| Device Name: | CELLMATIC CHLAMYDIA CULTURE CONFIRM-DIFCO-1000 |
| Classification | Cells, Animal And Human, Cultured |
| Applicant | DIFCO LABORATORIES, INC. 1180 ELLSWORTH RD. Ann Arbor, MI 48104 |
| Contact | Walter S Fisher |
| Correspondent | Walter S Fisher DIFCO LABORATORIES, INC. 1180 ELLSWORTH RD. Ann Arbor, MI 48104 |
| Product Code | KIR |
| CFR Regulation Number | 864.2280 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-01-28 |
| Decision Date | 1986-02-05 |