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

VAPOCIDE

K Number: K970726 · Decision May 18, 1998
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
62
Applicant Total
9
Review Days
444

Basic Information

Device Name
VAPOCIDE
K Number
K970726
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6885
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
COTTRELL, LTD.
Date Received
February 28, 1997
Decision Date
May 18, 1998
Product Code
MED
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
MED Sterilant, Medical Devices

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