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

COLDGEL

K Number: K953542 · Decision Oct 30, 1995
Classifications
1
FEI Numbers
377
Registration Numbers
377
Same Product Code
81
Applicant Total
5
Review Days
94

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Basic Information

Device Name
COLDGEL
K Number
K953542
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5710
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent for Some Indications
Applicant
Prism Technologies, Inc.
Date Received
July 28, 1995
Decision Date
October 30, 1995
Product Code
IMD
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IMD Pack, Hot Or Cold, Disposable

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Other Clearances by Prism Technologies, Inc.

K Number Device Name
K980212 MITYVAC
K953541 INSTANT COLDGEL
K934631 TRANSWARMER
K912715 INSTANT WARM GEL PACK