Pymah Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pymah Corp. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Pymah Corp. has 17 FDA 510(k) cleared medical devices. Based in Somerville, US.
Historical record: 17 cleared submissions from 1988 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pymah Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pymah Corp.
17 devices
Cleared
Feb 22, 1996
ATI ETHYLENE OXIDE STERILIZATION INDICATOR
General Hospital
239d
Cleared
Jul 06, 1995
ATI DISPOSABLE TEST PACK FOR STEAM STERILIZATION
General Hospital
45d
Cleared
May 10, 1995
ATI DISPOSABLE TEST PACK FOR EO GAS STERILIZATION
General Hospital
63d
Cleared
Apr 18, 1995
STERIGAGE EO 100%
General Hospital
553d
Cleared
Jan 27, 1995
TRIMLINE 2000
Cardiovascular
213d
Cleared
Feb 01, 1994
ATI DISPOSABLE BIOLOGICAL-PLUS TEST PACK
General Hospital
459d
Cleared
Feb 01, 1994
ATI(R) DISP BIOLOGICAL-PLUS TEST PACK
General Hospital
445d
Cleared
Nov 24, 1993
SLIMLINE 3000
Cardiovascular
89d
Cleared
Nov 17, 1993
GLUTARALDEHYDE MONITORS
General Hospital
427d
Cleared
Jul 30, 1993
TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF
Cardiovascular
259d
Cleared
Apr 30, 1993
BALANCED(TM) NYLON BLADDER
Cardiovascular
84d
Cleared
Jul 28, 1992
PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR
General Hospital
256d