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

REFEREE BLOOD GAS ANALYZER-ELECTRODES

K Number: K832779 · Decision Oct 14, 1983
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
186
Applicant Total
57
Review Days
59

Basic Information

Device Name
REFEREE BLOOD GAS ANALYZER-ELECTRODES
K Number
K832779
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1120
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
ANALYTICAL PRODUCTS, INC.
Date Received
August 16, 1983
Decision Date
October 14, 1983
Product Code
CHL
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
CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

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Other Clearances by ANALYTICAL PRODUCTS, INC.

K Number Device Name
K924814 API 20E/UNISCEPT 20E
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K922926 API UNISCEPT KB/TYPE 2 AND 3
K901559 MODIFICATION TO API UNISCEPT 20GP
K901390 DMAC INDOLE REAGENT
K895796 API UNISCEPT KB
K884510 MODIFICATION MICRO-MIC
K884509 MODIFICATION MIC/API UNISCEPT(R)
K880598 MODIFICATIONS TO API UNISCEPT (R) KB
K874466 API UNISCEPT(R) MICRO-MIC(R) SYSTEM/UNISCEPT MIC
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