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

CHEMDI-VHP CHEMICAL INDICATOR

K Number: K922485 · Decision Sep 29, 1993
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
36
Review Days
499

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CHEMDI-VHP CHEMICAL INDICATOR
K Number
K922485
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
American Sterilizer Co.
Date Received
May 18, 1992
Decision Date
September 29, 1993
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JOJ), ordered by most recent decision date.

View all

Other Clearances by American Sterilizer Co.

K Number Device Name
K943288 AMSCO SQ240 SURGICAL LIGHT
K931872 THE EAGLE 3017 100% ETHYLENE OXIDE STERILIZER
K930493 QUANTUM 3080 SURGICAL TABLE
K905816 ORTHOVISION TABLE
K896674 AMSCO QUANTUM LIGHT
K895164 EAGLE DS
K882660 GENERAL SURGICAL TABLE AND ACCESSORIES
K880198 GEMINI SURGICAL LIGHT
K864846 RADIOGRAPHIC - LEG SECTION
K844479 CHEMSPOR
Search all 36 clearances from American Sterilizer Co. →