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

ATI DISPOSABLE TEST PACK FOR EO GAS STERILIZATION

K Number: K951063 · Decision May 10, 1995
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
17
Review Days
63

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Basic Information

Device Name
ATI DISPOSABLE TEST PACK FOR EO GAS STERILIZATION
K Number
K951063
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pymah Corp.
Date Received
March 8, 1995
Decision Date
May 10, 1995
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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Other Clearances by Pymah Corp.

K Number Device Name
K952995 ATI ETHYLENE OXIDE STERILIZATION INDICATOR
K952408 ATI DISPOSABLE TEST PACK FOR STEAM STERILIZATION
K934874 STERIGAGE EO 100%
K943081 TRIMLINE 2000
K925745 ATI(R) DISP BIOLOGICAL-PLUS TEST PACK
K925496 ATI DISPOSABLE BIOLOGICAL-PLUS TEST PACK
K934180 SLIMLINE 3000
K924681 GLUTARALDEHYDE MONITORS
K925744 TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF
K930604 BALANCED(TM) NYLON BLADDER
Search all 17 clearances from Pymah Corp. →