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

MAM-CP X-RAY APPARATUS

K Number: K872980 · Decision Aug 27, 1987
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
7
Review Days
28

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Basic Information

Device Name
MAM-CP X-RAY APPARATUS
K Number
K872980
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Transworld X-Ray Corp.
Date Received
July 30, 1987
Decision Date
August 27, 1987
Product Code
IZH
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
IZH System, X-Ray, Mammographic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IZH), ordered by most recent decision date.

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Other Clearances by Transworld X-Ray Corp.

K Number Device Name
K892657 SENSIMAT
K890066 STAR 36
K873283 MODEL C2-5000 OVERHEAD TUBE SUPPORT
K872357 TRANSWORLD 360V, MODEL A1-4040
K841923 DCX-100 CHEST UNIT-GL-5000M
K827582 MODIFIED X-RAY TABLE