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

BG II ANALYZER

K Number: K771822 · Decision Oct 19, 1977
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
187
Applicant Total
157
Review Days
27

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
BG II ANALYZER
K Number
K771822
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1120
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Technicon Instruments Corp.
Date Received
September 22, 1977
Decision Date
October 19, 1977
Product Code
CHL
Advisory Committee
Clinical Chemistry
Review Advisory Committee
HE
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

Similar 510(k) Clearances

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

View all

Other Clearances by Technicon Instruments Corp.

K Number Device Name
K914511 TECHNICON AXON(TM) SYSTEM METHODS ANYALYE HDL CHOL
K914888 TECHNICON CHEM 1(TM) SYST (GEN2 SYST)
K914025 TECHNICON AXON(TM) SYSTEMS, ALT(P 5-P)/AST(P 5-P)
K912616 TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTES
K912413 CHEM-LINK DATA BASE MANAGER
K903825 DRUG OF ABUSE ANALYSIS SYSTEM
K903305 TECHNICON CHEM I SYSTEM CARBON DIOXIDE METHOD
K903824 DRUG OF ABUSE ANALYSIS SYSTEM FREE RADICAL ASSAY
K903306 TECHNICON CHEM I SYSTEM MAGNESIUM METHOD
K901410 TECHNICON RA-2000(TM) SYSTEM
Search all 157 clearances from Technicon Instruments Corp. →