510(k) K873262
K873262 is an FDA 510(k) premarket notification submitted by Central Media for the device "DIFFERENTIAL MEDIA". The FDA issued a decision of Substantially Equivalent on October 28, 1987. The device falls under product code JSI (Culture Media, Selective And Differential), a Class I device regulated under 21 CFR 866.2360. Central Media has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 28, 1987
- Date Received
- August 11, 1987
- 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