510(k) K854577

PRECEPT AMOXICILLIN/CLAVVLANIC ACID (AUGMENTIN) by Austin Biological Laboratories — Product Code JWY

K854577 is an FDA 510(k) premarket notification submitted by Austin Biological Laboratories for the device "PRECEPT AMOXICILLIN/CLAVVLANIC ACID (AUGMENTIN)". The FDA issued a decision of Substantially Equivalent on February 5, 1986. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Austin Biological Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 5, 1986
Date Received
October 23, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Manual Antimicrobial Susceptibility Test Systems
Device Class
Class II
Regulation Number
866.1640
Review Panel
MI
Submission Type