510(k) K823122
K823122 is an FDA 510(k) premarket notification submitted by Granite Diagnostics, Inc. for the device "LAKED BLOOD AGAR W/PAROMOMYCIN & VANCOM". The FDA issued a decision of Substantially Equivalent on December 3, 1982. The device falls under product code JSI (Culture Media, Selective And Differential), a Class I device regulated under 21 CFR 866.2360. Granite Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 3, 1982
- Date Received
- October 22, 1982
- 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