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

ECLIPSE PROBE COVER

K Number: K953673 · Decision Mar 14, 1996
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
30
Review Days
220

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Basic Information

Device Name
ECLIPSE PROBE COVER
K Number
K953673
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Parker Laboratories, Inc.
Date Received
August 7, 1995
Decision Date
March 14, 1996
Product Code
IYO
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
IYO System, Imaging, Pulsed Echo, Ultrasonic

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K864556 AQUALUBE(TM)
K861239 ACRYLIC SOLDER
K855167 DYNA SYSTEM
K851895 POLYGEL ULTRASOUND GEL
K852956 CONTACT CONDUCTIVE ADHESIVE GEL COMPOSITION
K841400 NEURO PULSE
K840548 RESIL
K831039 COMPLUS VARIOUS FORMS
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