FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

3M MEDICAL DIAGNOSTIC VIDEOCASSETTE

K Number: K931604 · Decision Jul 21, 1993
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
33
Applicant Total
49
Review Days
111

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Basic Information

Device Name
3M MEDICAL DIAGNOSTIC VIDEOCASSETTE
K Number
K931604
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1840
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3M Health Care, Ltd.
Date Received
April 1, 1993
Decision Date
July 21, 1993
Product Code
IWZ
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
IWZ Film, Radiographic

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K Number Device Name
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K941534 MODULAR VS-22 CEMENTED FEMORAL HIP SYSTEM
K941748 STERI-VAC GAS STERILIZER MODEL 8XL
K930681 3M PREVENTION FABRIC SURGICAL GOWN #78XX
K932307 3M MAXI-DRIVER II DBATTERY POWERED SYSTEM
K932422 3M TEGADERM HP TRANSPARENT DRESSING
K932446 INJECTION SITE
K931968 CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO
K933006 AVI INFUSION PUMPS, ADDITIONAL INTENDED USE
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