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

RADIOGRAPHIC GENERATOR HFQ-WHIS

K Number: K935068 · Decision Dec 13, 1993
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
162
Applicant Total
23
Review Days
49

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Basic Information

Device Name
RADIOGRAPHIC GENERATOR HFQ-WHIS
K Number
K935068
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bennett X-Ray Corp.
Date Received
October 25, 1993
Decision Date
December 13, 1993
Product Code
IZO
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
IZO Generator, High-Voltage, X-Ray, Diagnostic

Similar 510(k) Clearances

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

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Other Clearances by Bennett X-Ray Corp.

K Number Device Name
K964576 PROFILE MAMMOGRAPHY SYSTEM (M-PRO)
K952672 VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEM
K944978 BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSI
K945962 BENNETT X-RAY PROFILE POSITIONING PADDLE FOR MAMMOGRAPHY
K945731 HFQ HIGH FREQUENCY RADIOGRAPHIC AND FLUROSCOPIC GENERATORS
K945749 BENNETT X-RAY TOMOGRAPHY SYSTEM
K940701 BENNETT MAMMOGRAPHY POSITIONING CHAIR MODEL NO. M-PCH
K935649 WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY
K925725 CONTOUR MAMMOGRAPHY SYSTEM, MODEL NUMBER M-CTR
K925716 BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC
Search all 23 clearances from Bennett X-Ray Corp. →