FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MULTICHEM HDL PRECIPITATING REAGENT #S0914

K Number: K874820 · Decision Jan 7, 1988
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
65
Applicant Total
23
Review Days
44

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
MULTICHEM HDL PRECIPITATING REAGENT #S0914
K Number
K874820
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Simmler, Inc.
Date Received
November 24, 1987
Decision Date
January 7, 1988
Product Code
LBR
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
LBR Ldl & Vldl Precipitation, Hdl

Similar 510(k) Clearances

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

View all

Other Clearances by Simmler, Inc.

K Number Device Name
K895745 SICKLE CELL SOLUBILITY TEST KIT
K874903 MULTICHEM(R) Y -GLUTAMYLTRANSFERASE (Y -GT)
K874595 MULTICHEM (R) MAGNESIUM REAGENT
K874812 MULTICHEM CHLORIDE REAGENT S0933
K874311 MULTICHEM (R) TOTAL BILIRUBIN
K874049 MULTICHEM ALBUMIN REAGENT S0902
K874038 MULTICHEM INORGANIC PHOSPHOROUS S0923
K873725 MULTICHEM CREATININE REAGENT S0917
K873761 MULTICHEM ALKALINE PHOSPHATASE (S0903)
K873697 MULTICHEM CALCIUM S0910
Search all 23 clearances from Simmler, Inc. →