510(k) K880110
K880110 is an FDA 510(k) premarket notification submitted by Hardy Media for the device "CYSTINE TRYPTIC MEDIUM W/DEXTROSE". The FDA issued a decision of Substantially Equivalent on March 30, 1988. The device falls under product code JSF (Culture Media, Single Biochemical Test), a Class I device regulated under 21 CFR 866.2320. Hardy Media has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 30, 1988
- Date Received
- January 6, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Culture Media, Single Biochemical Test
- Device Class
- Class I
- Regulation Number
- 866.2320
- Review Panel
- MI
- Submission Type