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

CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITING DEVICE, MANUAL

K Number: K973833 · Decision Dec 30, 1997
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
235
Applicant Total
9
Review Days
84

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Basic Information

Device Name
CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITING DEVICE, MANUAL
K Number
K973833
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1720
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dynarad Corp.
Date Received
October 7, 1997
Decision Date
December 30, 1997
Product Code
IZL
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
IZL System, X-Ray, Mobile

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Other Clearances by Dynarad Corp.

K Number Device Name
K000052 X-RAY MONOBLOCK, MONOBLOCK XRS-60-330
K981267 FACTS MONOBLOCK
K932356 NOVA XM2
K941363 PHANTOM
K932353 HF-110A
K932355 9150A, 1100F
K932354 9170, 1170
K931725 ALPHA II