FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BLOOD UREA NITROGEN REAGENT

K Number: K792362 · Decision Dec 6, 1979
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
10
Applicant Total
14
Review Days
15

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BLOOD UREA NITROGEN REAGENT
K Number
K792362
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1770
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Connecticut Diagnostics, Ltd.
Date Received
November 21, 1979
Decision Date
December 6, 1979
Product Code
JGZ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JGZ O-Phthalaldehyde, Urea Nitrogen

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JGZ), ordered by most recent decision date.

View all

Other Clearances by Connecticut Diagnostics, Ltd.

K Number Device Name
K905617 VISI-STAPH
K822500 CDL LYSING REAGENT
K822501 CDL ISOTONIC DILUENT
K822504 CDL AUTO-LYSING REAGENT
K811222 INORGANIC PHOSPHORUS REAGENTS
K801898 URIC ACID DIAGNOSTIC REAGENT
K801897 GLUCOSE DIAGNOSTIC REAGENT
K792465 CONNECTICUT DIAGNOSTICS, LTS. DIRECT
K792338 DONNECT. DIAG. TOTAL BILIRUBIN REAGENTS
K792339 CONNECT. DIAG. ALBUMIN DIAGNOSTIC REAGEN
Search all 14 clearances from Connecticut Diagnostics, Ltd. →