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

WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY

K Number: K935649 · Decision Feb 9, 1994
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
23
Review Days
78

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Basic Information

Device Name
WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY
K Number
K935649
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bennett X-Ray Corp.
Date Received
November 23, 1993
Decision Date
February 9, 1994
Product Code
KPR
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
KPR System, X-Ray, Stationary

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Other Clearances by Bennett X-Ray Corp.

K Number Device Name
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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
K935068 RADIOGRAPHIC GENERATOR HFQ-WHIS
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. →