The following data is part of a premarket notification filed by Behring Diagnostics, Inc. with the FDA for Turbiquant Asl.
Device ID | K915742 |
510k Number | K915742 |
Device Name: | TURBIQUANT ASL |
Classification | Antistreptolysin - Titer/streptolysin O Reagent |
Applicant | BEHRING DIAGNOSTICS, INC. 17 CHUBB WAY Somerville, NJ 08876 |
Contact | John E Hughes |
Correspondent | John E Hughes BEHRING DIAGNOSTICS, INC. 17 CHUBB WAY Somerville, NJ 08876 |
Product Code | GTQ |
CFR Regulation Number | 866.3720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-12-23 |
Decision Date | 1993-06-28 |