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

PHASIX-HIGH FREQUENCY GENERATOR

K Number: K834306 · Decision Dec 29, 1983
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
39
Applicant Total
20
Review Days
55

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Basic Information

Device Name
PHASIX-HIGH FREQUENCY GENERATOR
K Number
K834306
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1760
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Cgr Medical Corp.
Date Received
November 4, 1983
Decision Date
December 29, 1983
Product Code
ITY
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
ITY Assembly, Tube Housing, X-Ray, Diagnostic

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Other Clearances by Cgr Medical Corp.

K Number Device Name
K843926 PRESTILIX 1690
K843235 STENOSCOP
K843985 SUSPENSION 7
K841649 MAXIMAX - 4
K833223 SONEL 3000A
K833941 ORION
K833846 PROCESS 100 ST
K837412 SATURNE I LINEAR ACCELERATOR
K837465 ALCYON ROTATIONAL COBALT THERAPY
K837336 VERASUN RADIATION THERAPY SIMULATION SYSTEM
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