The following data is part of a premarket notification filed by Analytical Control Systems, Inc. with the FDA for Acs Liquid Thromboplastin.
Device ID | K912102 |
510k Number | K912102 |
Device Name: | ACS LIQUID THROMBOPLASTIN |
Classification | Test, Time, Prothrombin |
Applicant | ANALYTICAL CONTROL SYSTEMS, INC. 155 E. MARKET, SUITE 502 Indianapolis, IN 46204 |
Contact | Pauline W Bonderman |
Correspondent | Pauline W Bonderman ANALYTICAL CONTROL SYSTEMS, INC. 155 E. MARKET, SUITE 502 Indianapolis, IN 46204 |
Product Code | GJS |
CFR Regulation Number | 864.7750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-05-13 |
Decision Date | 1991-08-09 |