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

MAMMOGRAPHIC MODEL CXR 51 MO-6'/0.6 SH

K Number: K864042 · Decision Oct 27, 1986
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
39
Applicant Total
3
Review Days
11

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Basic Information

Device Name
MAMMOGRAPHIC MODEL CXR 51 MO-6'/0.6 SH
K Number
K864042
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1760
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Absolute X-Ray Corp.
Date Received
October 16, 1986
Decision Date
October 27, 1986
Product Code
ITY
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
ITY Assembly, Tube Housing, X-Ray, Diagnostic

Similar 510(k) Clearances

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Other Clearances by Absolute X-Ray Corp.

K Number Device Name
K881387 X-RAY GENERATING SYSTEM, TF 800
K854486 TABLE,RADIOGRAPHIC-FLUOROSCOPIC,TOMOGRAPHIC,REMOTE