The following data is part of a premarket notification filed by Creative Laboratory Products, Inc. with the FDA for Clp Activated Partial Thromboplastin Time Test.
Device ID | K881068 |
510k Number | K881068 |
Device Name: | CLP ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST |
Classification | Activated Partial Thromboplastin |
Applicant | CREATIVE LABORATORY PRODUCTS, INC. 6258 LA PAS TRAIL Indianapolis, IN 46268 |
Contact | Roy Speck |
Correspondent | Roy Speck CREATIVE LABORATORY PRODUCTS, INC. 6258 LA PAS TRAIL Indianapolis, IN 46268 |
Product Code | GFO |
CFR Regulation Number | 864.7925 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-03-14 |
Decision Date | 1988-03-23 |