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

VIS-U-ALL II SELF SEAL POUCH

K Number: K070765 · Decision Oct 12, 2007
Classifications
1
FEI Numbers
265
Registration Numbers
265
Same Product Code
270
Applicant Total
169
Review Days
206

Basic Information

Device Name
VIS-U-ALL II SELF SEAL POUCH
K Number
K070765
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STERIS Corporation
Date Received
March 20, 2007
Decision Date
October 12, 2007
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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