The following data is part of a premarket notification filed by Boots-celltech Diagnostics, Inc. with the FDA for Imagen(tm) Chlamydia Specimen Collection Kit.
Device ID | K862607 |
510k Number | K862607 |
Device Name: | IMAGEN(TM) CHLAMYDIA SPECIMEN COLLECTION KIT |
Classification | Device, Specimen Collection |
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 | LIO |
CFR Regulation Number | 866.2900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-07-08 |
Decision Date | 1986-08-04 |