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

SULTAN SPOROX TEST VIAL, MODEL 75195

K Number: K020612 · Decision May 7, 2002
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
262
Applicant Total
11
Review Days
71

Basic Information

Device Name
SULTAN SPOROX TEST VIAL, MODEL 75195
K Number
K020612
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SULTAN CHEMISTS, INC.
Date Received
February 25, 2002
Decision Date
May 7, 2002
Product Code
JOJ
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
JOJ Indicator, Physical/Chemical Sterilization Process

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