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

ASSURE SELF SEALING STERILIZATION POUCH

K Number: K933729 · Decision Jun 21, 1994
Classifications
1
FEI Numbers
265
Registration Numbers
265
Same Product Code
270
Applicant Total
11
Review Days
323

Basic Information

Device Name
ASSURE SELF SEALING STERILIZATION POUCH
K Number
K933729
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SULTAN CHEMISTS, INC.
Date Received
August 2, 1993
Decision Date
June 21, 1994
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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K030414 GENIE ULTRA HYDROPHILIC IMPRESSION MATERIAL
K020612 SULTAN SPOROX TEST VIAL, MODEL 75195
K002843 SULTAN SENSITEMP RESIN TEMPORARY CEMENT, MODEL 70010
K991509 PRO-PORTION CLEANER/DISINFECTANT
K971138 DINABASE (TM)
K951590 ASSURE, SELF-SEALING STERILIZATION POUCH
K896826 SULTAN PERIO-SELECT IRRIGATION SYSTEM
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