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

MULTICARE PLATINUM SYSTEM AND ACCESSORIES

K Number: K030666 · Decision Mar 25, 2003
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
5
Review Days
22

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Basic Information

Device Name
MULTICARE PLATINUM SYSTEM AND ACCESSORIES
K Number
K030666
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lorad, A Hologic Co.
Date Received
March 3, 2003
Decision Date
March 25, 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 Lorad, A Hologic Co.

K Number Device Name
K122836 AFFIRM BREAST BIOPSY GUIDANCE SYSTEM
K071542 DIGITAL STEREOLOC II
K013290 MODIFIED 650 MAMMOGRAPHY SYSTEM
K011987 MODIFIED M-IV MAMMOGRAPHY SYSTEM