Pymah Corp.
Pymah Corp. appears in FDA public data with 0 recalls, 17 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Feb 22, 1996.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 17
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K952995 | ATI ETHYLENE OXIDE STERILIZATION INDICATOR | Feb 22, 1996 |
| K952408 | ATI DISPOSABLE TEST PACK FOR STEAM STERILIZATION | Jul 6, 1995 |
| K951063 | ATI DISPOSABLE TEST PACK FOR EO GAS STERILIZATION | May 10, 1995 |
| K934874 | STERIGAGE EO 100% | Apr 18, 1995 |
| K943081 | TRIMLINE 2000 | Jan 27, 1995 |
| K925745 | ATI(R) DISP BIOLOGICAL-PLUS TEST PACK | Feb 1, 1994 |
| K925496 | ATI DISPOSABLE BIOLOGICAL-PLUS TEST PACK | Feb 1, 1994 |
| K934180 | SLIMLINE 3000 | Nov 24, 1993 |
| K924681 | GLUTARALDEHYDE MONITORS | Nov 17, 1993 |
| K925744 | TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF | Jul 30, 1993 |
| K930604 | BALANCED(TM) NYLON BLADDER | Apr 30, 1993 |
| K915170 | PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR | Jul 28, 1992 |
| K903379 | PYMAH PRE-GAGED BALANCED TEMPA-KUFF | Oct 19, 1990 |
| K894399 | STERIGAGE INTEGRATOR TEST PACK FOR STEAM STERILI. | Sep 11, 1989 |
| K894398 | STERIGAGE INTEGRATOR TEST PACK FOR ETHYLENE OXIDE | Sep 11, 1989 |
| K884421 | PRE-GAGED BALANCED CUFF W/SYLGARD ANTIMICRO. TREAT | Jan 13, 1989 |
| K881286 | TEMPA-DOT CLINICAL THERMOMETER SHEATH | Jun 8, 1988 |