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

BROWNE STEAM INDICATOR

K Number: K970918 · Decision Jun 24, 1997
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
5
Review Days
104

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Basic Information

Device Name
BROWNE STEAM INDICATOR
K Number
K970918
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Board of Directors, Albert Browne , Ltd.
Date Received
March 12, 1997
Decision Date
June 24, 1997
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.

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Other Clearances by Board of Directors, Albert Browne , Ltd.

K Number Device Name
K971971 BROWNE TST SINGLE USE BOWIE-DICK TYPE TEST PACK
K932057 BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK
K922481 BROWNE GA INDICATOR USE IN 2% ACTIV GLUTARALDEHYDE
K902958 TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE