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

SHIMADZU COLLIMATOR R-30H

K Number: K031771 · Decision Aug 21, 2003
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
16
Applicant Total
49
Review Days
73

Basic Information

Device Name
SHIMADZU COLLIMATOR R-30H
K Number
K031771
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.1610
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SHIMADZU CORP.
Date Received
June 9, 2003
Decision Date
August 21, 2003
Product Code
IZX
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
IZX Collimator, Manual, Radiographic

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K101036 SHIMADZU COLLIMATOR R-20J
K090578 SHIMADZU COLLIMATOR R-30H
K090268 SHIMADZU MOBILE X-RAY SYSTEM MOBILE ART EVOLUTION
K080701 SHIMADZU MOBILE X-RAY SYSTEM MOBILEDART EVOLUTION
K072006 DAR-9400F
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K062360 BRANSIST SAFIRE
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