Penlon, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Penlon, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SIGMA ELITE, PENLON BREATHING SYSTEM PRESSURE MONITOR, PENLON IDP PRESSURE FAILURE ALARM
10
Total
10
Cleared
0
Denied
Penlon, Inc. has 10 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1980 to 1994.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Penlon, Inc.
10 devices
Cleared
Nov 04, 1994
SIGMA ELITE
Anesthesiology
319d
Cleared
Aug 17, 1990
PENLON BREATHING SYSTEM PRESSURE MONITOR
Toxicology
79d
Cleared
Aug 10, 1989
PENLON IDP PRESSURE FAILURE ALARM
Anesthesiology
17d
Cleared
Mar 12, 1985
PENLON PPV VAPORIZER
Anesthesiology
151d
Cleared
Mar 12, 1985
PENLON AM1000 ANAESTHESIA MACHINE
Anesthesiology
151d
Cleared
Jan 05, 1983
MAGTARAK RESPIRATORY MONITOR & FLOW SENS
Anesthesiology
35d
Cleared
Jan 07, 1981
NUFFIELD ANESTHESIA VENTILATOR SER. 400
Anesthesiology
36d
Cleared
Jan 02, 1981
CREST ELECTRONIC WARMING BLANKET
Cardiovascular
219d
Cleared
Jun 09, 1980
PENLON I.D.P. PRESSSURE FAILURE ALARM
Anesthesiology
12d
Cleared
Jun 04, 1980
PENLON JUMBO CARBON DIOXIDE ABSORBER
Anesthesiology
7d