The following data is part of a premarket notification filed by Analytical Control Systems, Inc. with the FDA for Acs Ultra-2 Thromboplastin.
Device ID | K913250 |
510k Number | K913250 |
Device Name: | ACS ULTRA-2 THROMBOPLASTIN |
Classification | Test, Time, Prothrombin |
Applicant | ANALYTICAL CONTROL SYSTEMS, INC. 9058 TECHNOLOGY DR. Fishers, IN 46038 |
Contact | Pauline Bonderman |
Correspondent | Pauline Bonderman ANALYTICAL CONTROL SYSTEMS, INC. 9058 TECHNOLOGY DR. Fishers, IN 46038 |
Product Code | GJS |
CFR Regulation Number | 864.7750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-07-22 |
Decision Date | 1991-11-27 |