510(k) K781885
K781885 is an FDA 510(k) premarket notification submitted by Fisher Scientific Co., LLC for the device "SERUM, BLOOD UREA NITIOGEN". The FDA issued a decision of Substantially Equivalent on December 20, 1978. The device falls under product code CDW (Diacetyl-Monoxime, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Fisher Scientific Co., LLC has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 20, 1978
- Date Received
- November 7, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Diacetyl-Monoxime, Urea Nitrogen
- Device Class
- Class II
- Regulation Number
- 862.1770
- Review Panel
- CH
- Submission Type