510(k) K872686
K872686 is an FDA 510(k) premarket notification submitted by I.A.F. Production, Inc. for the device "IAFP MUELLER HINTON AGAR". The FDA issued a decision of Substantially Equivalent on August 11, 1987. The device falls under product code LKA (Culture Media, Antimicrobial Susceptibility Test), a Class II device regulated under 21 CFR 866.1700. I.A.F. Production, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 11, 1987
- Date Received
- July 7, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Culture Media, Antimicrobial Susceptibility Test
- Device Class
- Class II
- Regulation Number
- 866.1700
- Review Panel
- MI
- Submission Type