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

ULTRA-VIOLET BUN REAGENT KIT

K Number: K851513 · Decision May 20, 1985
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
116
Applicant Total
19
Review Days
35

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
ULTRA-VIOLET BUN REAGENT KIT
K Number
K851513
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1770
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Bio-Analytics Laboratories, Inc.
Date Received
April 15, 1985
Decision Date
May 20, 1985
Product Code
CDQ
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
CDQ Urease And Glutamic Dehydrogenase, Urea Nitrogen

Similar 510(k) Clearances

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

View all

Other Clearances by Bio-Analytics Laboratories, Inc.

K Number Device Name
K861638 KINETIC ALKALINE PHOSPHATASE REAGENT KIT
K860245 ENZYMATIC ALPHA-AMYLASE REAGENT KIT
K860213 ALBUMIN REAGENT KIT
K851514 ULTRA-VIOLET GLUCOSE REAGENT
K850639 ENZYMATIC ALPHA-AMYLASE REAGENT KIT
K832771 ERYTHROCYTE TEST
K832567 ACETAMINOPHEN(PARACETAMOL
K831414 COLORIMETRIC BUN
K821934 BIO-CAL OPERATION CHECK KIT
K813431 SALICYLATES
Search all 19 clearances from Bio-Analytics Laboratories, Inc. →