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

MPG-50 X-RAY GENERATOR

K Number: K873544 · Decision Oct 26, 1987
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
162
Applicant Total
3
Review Days
55

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Basic Information

Device Name
MPG-50 X-RAY GENERATOR
K Number
K873544
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Thomson-Cgr Medical Corp.
Date Received
September 1, 1987
Decision Date
October 26, 1987
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 Thomson-Cgr Medical Corp.

K Number Device Name
K873618 STEREOTIX
K852353 DG 200/300 DIGITAL ANGIOGRAPHIC SYSTEM