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

WONDER WARMER

K Number: K810633 · Decision Mar 26, 1981
Classifications
1
FEI Numbers
377
Registration Numbers
377
Same Product Code
81
Applicant Total
1
Review Days
16

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Basic Information

Device Name
WONDER WARMER
K Number
K810633
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5710
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Montvale Products, Inc.
Date Received
March 10, 1981
Decision Date
March 26, 1981
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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