510(k) K801805
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