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

PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA

K Number: K031114 · Decision Mar 3, 2004
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
3
Applicant Total
15
Review Days
330

Basic Information

Device Name
PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA
K Number
K031114
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
RAVEN BIOLOGICAL LABORATORIES, INC.
Date Received
April 8, 2003
Decision Date
March 3, 2004
Product Code
MRB
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
MRB Indicator, Biological, Liquid Chemical Sterilization Process

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