510(k) K792362
K792362 is an FDA 510(k) premarket notification submitted by Connecticut Diagnostics, Ltd. for the device "BLOOD UREA NITROGEN REAGENT". The FDA issued a decision of Substantially Equivalent on December 6, 1979. The device falls under product code JGZ (O-Phthalaldehyde, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Connecticut Diagnostics, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 6, 1979
- Date Received
- November 21, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- O-Phthalaldehyde, Urea Nitrogen
- Device Class
- Class II
- Regulation Number
- 862.1770
- Review Panel
- CH
- Submission Type