510(k) K915742

TURBIQUANT ASL by Behring Diagnostics, Inc. — Product Code GTQ

K915742 is an FDA 510(k) premarket notification submitted by Behring Diagnostics, Inc. for the device "TURBIQUANT ASL". The FDA issued a decision of Substantially Equivalent on June 28, 1993. The device falls under product code GTQ (Antistreptolysin - Titer/Streptolysin O Reagent), a Class I device regulated under 21 CFR 866.3720. Behring Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 28, 1993
Date Received
December 23, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antistreptolysin - Titer/Streptolysin O Reagent
Device Class
Class I
Regulation Number
866.3720
Review Panel
MI
Submission Type