510(k) K850379
K850379 is an FDA 510(k) premarket notification submitted by Advanced Biomedical Methods, Inc. for the device "DIRECT BILIRUBIN FOR DEMAND ANALYZER". The FDA issued a decision of Substantially Equivalent on March 1, 1985. The device falls under product code CIG (Diazo Colorimetry, Bilirubin), a Class II device regulated under 21 CFR 862.1110. Advanced Biomedical Methods, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 1, 1985
- Date Received
- January 31, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Diazo Colorimetry, Bilirubin
- Device Class
- Class II
- Regulation Number
- 862.1110
- Review Panel
- CH
- Submission Type