510(k) K831414
K831414 is an FDA 510(k) premarket notification submitted by Bio-Analytics Laboratories, Inc. for the device "COLORIMETRIC BUN". The FDA issued a decision of Substantially Equivalent on June 16, 1983. The device falls under product code CDL (Berthelot Indophenol, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Bio-Analytics Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 16, 1983
- Date Received
- May 2, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Berthelot Indophenol, Urea Nitrogen
- Device Class
- Class II
- Regulation Number
- 862.1770
- Review Panel
- CH
- Submission Type