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

MAMMOGRAPHIC KVP METER MODEL 232

K Number: K873836 · Decision Oct 16, 1987
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
12
Review Days
25

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Basic Information

Device Name
MAMMOGRAPHIC KVP METER MODEL 232
K Number
K873836
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Radiation Measurements, Inc.
Date Received
September 21, 1987
Decision Date
October 16, 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 Radiation Measurements, Inc.

K Number Device Name
K893216 RMI ULTRASOUND DOPPLER PHANTOM SYSTEM
K885223 RMI SHORT DISTANCE ALIGNMENT DEVICE
K873956 ULTIMETER
K854976 RMI RESPIRATORY GATING SYSTEM MODEL 301
K834483 DIGI-X
K834607 ELECTRONIC KVP CASSETTE
K834482 TISSUE MIMICKING ULTRASOUND PHANTOMS
K834481 DOPPLER PHANTOM FLOW CONTROL SYS
K837033 ROTATABLE HALF BEAM SHIELDING BLOCK MODEL 440
K812949 RMI TRANSILLUMINATOR, MODEL 292
Search all 12 clearances from Radiation Measurements, Inc. →