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

CARBON DIOXIDE REAGENT

K Number: K881169 · Decision Apr 28, 1988
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
85
Applicant Total
21
Review Days
41

Basic Information

Device Name
CARBON DIOXIDE REAGENT
K Number
K881169
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1160
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
INTERSECT SYSTEMS, INC.
Date Received
March 18, 1988
Decision Date
April 28, 1988
Product Code
KHS
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
KHS Enzymatic, Carbon-Dioxide

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Other Clearances by INTERSECT SYSTEMS, INC.

K Number Device Name
K021636 ALBUMIN REAGENT
K011972 DIRECT BILIRUBIN REAGENT
K011692 HOMOGENEOUS ENZYMIC HOMOCYSTEINE REAGENT
K003892 TOTAL BILIRUBIN REAGENT
K983937 DUAL VIAL CREATININE REAGENT
K974833 CK-NAC REAGENT
K941807 INTERSECT SYSTEMS' NON-MERCURIC CHLORIDE REAGENT
K932888 INTERSECT SYSTEMS DIRECT AMYLASE REAGENT
K934039 INTERSECT SYSTEMS HDL CHOLESTEROL REAGENT SET
K932267 ENZYMATIC CO2 REAGENT, MODIFICATION
Search all 21 clearances from INTERSECT SYSTEMS, INC. →