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

LINDE OXYGEN THERAPY FLOWMETERS, L33-L34

K Number: K791069 · Decision Jun 27, 1979
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
23
Applicant Total
69
Review Days
15

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Basic Information

Device Name
LINDE OXYGEN THERAPY FLOWMETERS, L33-L34
K Number
K791069
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.2340
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Union Carbide Corp.
Date Received
June 12, 1979
Decision Date
June 27, 1979
Product Code
CAX
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CAX Flowmeter, Tube, Thorpe, Back-Pressure Compensated

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Other Clearances by Union Carbide Corp.

K Number Device Name
K830337 MARK III OXYGEN WALKER SYS-LOW PRESS
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K820535 LASER GAS MIXTURES
K812536 LINDE MARK II
K810732 LINDE MARK II OXYGEN RESERV. TYPE OR-4
K810596 CENTRIFI CHEM SYSTEM 400 ANALYZER
K810129 CENTRIFICHEM SYSTEM 500
K803216 CENTRIFICHEM AST/SGOT OPTIMIZED REAGENT
K802741 CENTRIFICHEM COMB. SERUM-BASED CALIB.
K802520 CENTRIFICHEM PIPETTOR ACCURACY CALIB.
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