510(k) K771814
K771814 is an FDA 510(k) premarket notification submitted by Ortho Diagnostics, Inc. for the device "REAGENT CONFIDENCE SERA". The FDA issued a decision of Substantially Equivalent on November 7, 1977. The device falls under product code KSF (Kit, Quality Control For Blood Banking Reagents), a Class II device regulated under 21 CFR 864.9650. Ortho Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 7, 1977
- Date Received
- September 27, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Quality Control For Blood Banking Reagents
- Device Class
- Class II
- Regulation Number
- 864.9650
- Review Panel
- HE
- Submission Type