510(k) K863789
K863789 is an FDA 510(k) premarket notification submitted by Corning Medical & Scientific for the device "CORNING ELISA PLATES". The FDA issued a decision of Substantially Equivalent on October 3, 1986. The device falls under product code LIB (Device, General Purpose, Microbiology, Diagnostic), a Class I device regulated under 21 CFR 866.2660. Corning Medical & Scientific has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 3, 1986
- Date Received
- September 26, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, General Purpose, Microbiology, Diagnostic
- Device Class
- Class I
- Regulation Number
- 866.2660
- Review Panel
- MI
- Submission Type