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

BENNETT X-RAY TOMOGRAPHY SYSTEM

K Number: K945749 · Decision Feb 15, 1995
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
41
Applicant Total
23
Review Days
84

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Basic Information

Device Name
BENNETT X-RAY TOMOGRAPHY SYSTEM
K Number
K945749
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1740
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bennett X-Ray Corp.
Date Received
November 23, 1994
Decision Date
February 15, 1995
Product Code
IZF
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
IZF System, X-Ray, Tomographic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IZF), 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
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
K925716 BENNETT OVERHEAD TUBE CRANE MODEL NO. B-OTC
Search all 23 clearances from Bennett X-Ray Corp. →