FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PROVIEW SELF-SEALING STERILIZATION POUCH

K Number: K893802 · Decision Apr 4, 1990
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
9
Review Days
317

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Basic Information

Device Name
PROVIEW SELF-SEALING STERILIZATION POUCH
K Number
K893802
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Cottrell, Ltd.
Date Received
May 22, 1989
Decision Date
April 4, 1990
Product Code
KCT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

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K952234 BARRIER ALL FILM
K932922 PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR
K951983 IMNI-II
K945575 PRO BARRIER(TM) TUBE SOX(TM)