The following data is part of a premarket notification filed by Technology Management & Marketing, Inc. with the FDA for Gonostat Female Specimen Collection & Transport.
Device ID | K872325 |
510k Number | K872325 |
Device Name: | GONOSTAT FEMALE SPECIMEN COLLECTION & TRANSPORT |
Classification | System, Transport, Aerobic |
Applicant | TECHNOLOGY MANAGEMENT & MARKETING, INC. 333 WEST WACKER DR. SUITE 1900 Chicago, IL 60606 |
Contact | A Marcouiller |
Correspondent | A Marcouiller TECHNOLOGY MANAGEMENT & MARKETING, INC. 333 WEST WACKER DR. SUITE 1900 Chicago, IL 60606 |
Product Code | JTW |
CFR Regulation Number | 866.2900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-06-17 |
Decision Date | 1987-08-12 |