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

BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC

K Number: K914944 · Decision Dec 2, 1991
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
39
Applicant Total
23
Review Days
28

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Basic Information

Device Name
BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC
K Number
K914944
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1770
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bennett X-Ray Corp.
Date Received
November 4, 1991
Decision Date
December 2, 1991
Product Code
IYB
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
IYB Tube Mount, X-Ray, Diagnostic

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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
K935068 RADIOGRAPHIC GENERATOR HFQ-WHIS
K925725 CONTOUR MAMMOGRAPHY SYSTEM, MODEL NUMBER M-CTR
Search all 23 clearances from Bennett X-Ray Corp. →