510(k) K881555
K881555 is an FDA 510(k) premarket notification submitted by Acumedia Manufacturers, Inc. for the device "TINSDALE AGAR BASE". The FDA issued a decision of Substantially Equivalent on Apr 18, 1988. The device falls under product code JSI (Culture Media, Selective And Differential), a Class I device regulated under 21 CFR 866.2360. Acumedia Manufacturers, Inc. has 176 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 18, 1988
- Date Received
- Apr 8, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Culture Media, Selective And Differential
- Device Class
- Class I
- Regulation Number
- 866.2360
- Review Panel
- MI
- Submission Type
- 510(k) Exempt