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

ICE CONTAINER I.C.E.

K Number: K792182 · Decision Nov 15, 1979
Classifications
1
FEI Numbers
467
Registration Numbers
468
Same Product Code
26
Applicant Total
27
Review Days
17

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Basic Information

Device Name
ICE CONTAINER I.C.E.
K Number
K792182
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5700
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Delta Medical Industries
Date Received
October 29, 1979
Decision Date
November 15, 1979
Product Code
IME
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
IME Pack, Hot Or Cold, Reusable

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K831750 PM-3
K822761 DELIVERY TUBE SET #2226
K820912 PMS-2 PRESSURE MONITOR SEPARATOR
K820482 ACCU-RYNGE INSULIN PUMP #SP-250
K810068 PEDIATRIC ARTERIAL BLOOD FILTER
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