Pymah Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K952995ATI ETHYLENE OXIDE STERILIZATION INDICATORFebruary 22, 1996
K952408ATI DISPOSABLE TEST PACK FOR STEAM STERILIZATIONJuly 6, 1995
K951063ATI DISPOSABLE TEST PACK FOR EO GAS STERILIZATIONMay 10, 1995
K934874STERIGAGE EO 100%April 18, 1995
K943081TRIMLINE 2000January 27, 1995
K925496ATI DISPOSABLE BIOLOGICAL-PLUS TEST PACKFebruary 1, 1994
K925745ATI(R) DISP BIOLOGICAL-PLUS TEST PACKFebruary 1, 1994
K934180SLIMLINE 3000November 24, 1993
K924681GLUTARALDEHYDE MONITORSNovember 17, 1993
K925744TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFFJuly 30, 1993
K930604BALANCED(TM) NYLON BLADDERApril 30, 1993
K915170PYMAH COLD STERILOG GLUTARALDEHYDE MONITORJuly 28, 1992
K903379PYMAH PRE-GAGED BALANCED TEMPA-KUFFOctober 19, 1990
K894398STERIGAGE INTEGRATOR TEST PACK FOR ETHYLENE OXIDESeptember 11, 1989
K894399STERIGAGE INTEGRATOR TEST PACK FOR STEAM STERILI.September 11, 1989
K884421PRE-GAGED BALANCED CUFF W/SYLGARD ANTIMICRO. TREATJanuary 13, 1989
K881286TEMPA-DOT CLINICAL THERMOMETER SHEATHJune 8, 1988