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

SQUEEZE-EASE MAMMOGRAPHY CUSHION

K Number: K031574 · Decision Aug 4, 2003
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
4
Review Days
76

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Basic Information

Device Name
SQUEEZE-EASE MAMMOGRAPHY CUSHION
K Number
K031574
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
S & S X-Ray Products, Inc.
Date Received
May 20, 2003
Decision Date
August 4, 2003
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 S & S X-Ray Products, Inc.

K Number Device Name
K944040 PLANET THERMOPLASTIC IMMOBILIZATION SYSTEM
K883317 DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST
K850614 SAND S MB12 MAMMOGRAPHY MOVING GRID BUCKY