510(k) K960313
K960313 is an FDA 510(k) premarket notification submitted by Remel, L.P. for the device "MUELLER HINTON AGAR WITH 2% NACI". The FDA issued a decision of Substantially Equivalent on March 25, 1996. The device falls under product code JTZ (Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth), a Class II device regulated under 21 CFR 866.1700. Remel, L.P. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 25, 1996
- Date Received
- January 22, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth
- Device Class
- Class II
- Regulation Number
- 866.1700
- Review Panel
- MI
- Submission Type