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

ALLEGIANCE KWIK HEAT WARM PERINEAL PACK

K Number: K973770 · Decision Nov 13, 1997
Classifications
1
FEI Numbers
377
Registration Numbers
377
Same Product Code
81
Applicant Total
63
Review Days
42

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Basic Information

Device Name
ALLEGIANCE KWIK HEAT WARM PERINEAL PACK
K Number
K973770
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5710
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Allegiance Healthcare Corp.
Date Received
October 2, 1997
Decision Date
November 13, 1997
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

Similar 510(k) Clearances

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Other Clearances by Allegiance Healthcare Corp.

K Number Device Name
K023673 AIRLIFE DEMAND NASAL CANNULA
K023419 TRILAMINATE DRAPES/TIBURON
K024120 MODIFICATION TO TEMNO BIOPSY NEEDLES
K024292 MODIFICATION TO POSITIVE TOUCH POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN AND CHEMOTHERAPY LABELING CLAIM
K024102 DENTAL POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM
K023425 DRAPES WITH ABSORBENT REINFORCEMENT
K022765 NITRILE POWDER-FREE EXAMINATION GLOVES
K023170 NITRILE POWDER-FREE EXAMINATION GLOVES
K023167 BREATHABLE SURGICAL GOWN
K012931 GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM
Search all 63 clearances from Allegiance Healthcare Corp. →