Pymah Corp.
Pymah Corp. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1996.
Top product codes for Pymah Corp.
Recent clearances by Pymah Corp.
- K952995 — ATI ETHYLENE OXIDE STERILIZATION INDICATOR
- K952408 — ATI DISPOSABLE TEST PACK FOR STEAM STERILIZATION
- K951063 — ATI DISPOSABLE TEST PACK FOR EO GAS STERILIZATION
- K934874 — STERIGAGE EO 100%
- K943081 — TRIMLINE 2000
- K925496 — ATI DISPOSABLE BIOLOGICAL-PLUS TEST PACK
- K925745 — ATI(R) DISP 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
- K915170 — PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR
- K903379 — PYMAH PRE-GAGED BALANCED TEMPA-KUFF
- K894398 — STERIGAGE INTEGRATOR TEST PACK FOR ETHYLENE OXIDE
- K894399 — STERIGAGE INTEGRATOR TEST PACK FOR STEAM STERILI.
- K884421 — PRE-GAGED BALANCED CUFF W/SYLGARD ANTIMICRO. TREAT
- K881286 — TEMPA-DOT CLINICAL THERMOMETER SHEATH
Data sourced from openFDA. This site is unofficial and independent of the FDA.