510(k) K901598
K901598 is an FDA 510(k) premarket notification submitted by Microtech Medical Systems, Inc. for the device "FASTIDIOUS MIC PANEL". The FDA issued a decision of Substantially Equivalent on November 8, 1990. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Microtech Medical Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 8, 1990
- Date Received
- April 5, 1990
- 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