Medical Device Manufacturer · US , Menomonee Falls , WI

Pryon Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1992
4
Total
4
Cleared
0
Denied

Pryon Corp. has 4 FDA 510(k) cleared medical devices. Based in Menomonee Falls, US.

Historical record: 4 cleared submissions from 1992 to 1994. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Pryon Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pryon Corp.
4 devices
1-4 of 4
Cleared Jul 25, 1994
A-200 MULTI-USE AIRWAY ADAPTER
K942772 · CCK
Anesthesiology · 42d
Cleared Jul 13, 1994
CAP 400 AT
K935272 · CCK
Anesthesiology · 253d
Cleared Oct 15, 1993
LOW DEAD SPACE ADAPTOR & REUASABLE AIRWAY ADAPTOR
K930250 · CCK
Anesthesiology · 282d
Cleared Jun 24, 1992
P-300 CAPNOGRAPH AND PULSE OXIMETER
K915773 · DQA
Anesthesiology · 183d
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