510(k) K822334
K822334 is an FDA 510(k) premarket notification submitted by Gilford Diagnostics for the device "BILIRUBIN CALIBRATORS". The FDA issued a decision of Substantially Equivalent on September 2, 1982. The device falls under product code JIT (Calibrator, Secondary), a Class II device regulated under 21 CFR 862.1150. Gilford Diagnostics has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 2, 1982
- Date Received
- August 4, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Calibrator, Secondary
- Device Class
- Class II
- Regulation Number
- 862.1150
- Review Panel
- CH
- Submission Type