The following data is part of a premarket notification filed by Boots-celltech Diagnostics, Inc. with the FDA for Modified Imagen(tm) Chlamydia Test.
| Device ID | K864539 |
| 510k Number | K864539 |
| Device Name: | MODIFIED IMAGEN(TM) CHLAMYDIA TEST |
| Classification | Antiserum, Fluorescent, Chlamydia Trachomatis |
| Applicant | BOOTS-CELLTECH DIAGNOSTICS, INC. 240 BATH ROAD SLOUGH SL1 4ET Berkshire, England, GB |
| Contact | John G Simpson |
| Correspondent | John G Simpson BOOTS-CELLTECH DIAGNOSTICS, INC. 240 BATH ROAD SLOUGH SL1 4ET Berkshire, England, GB |
| Product Code | LJP |
| CFR Regulation Number | 866.3120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-11-19 |
| Decision Date | 1987-03-12 |