510(k) K801805

METRONIDAZOLE DISCS by G.D. Searle and Co. — Product Code JWY

K801805 is an FDA 510(k) premarket notification submitted by G.D. Searle and Co. for the device "METRONIDAZOLE DISCS". The FDA issued a decision of Substantially Equivalent on February 10, 1981. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. G.D. Searle and Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 10, 1981
Date Received
July 29, 1980
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