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

RECOVER INFANT HEEL WARMER (5100)

K Number: K964523 · Decision Feb 10, 1997
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
10
Applicant Total
2
Review Days
90

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Basic Information

Device Name
RECOVER INFANT HEEL WARMER (5100)
K Number
K964523
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5710
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Florida Medical Industries, Inc.
Date Received
November 12, 1996
Decision Date
February 10, 1997
Product Code
MPO
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
MPO Infant Heel Warmer (Chemical Heat Pack)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MPO), ordered by most recent decision date.

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Other Clearances by Florida Medical Industries, Inc.

K Number Device Name
K963689 RECOVER ADULT VEIN WARMER