Medical Device Manufacturer · US , Mchenry , IL

Diemolding Corp. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1976

Total

Cleared

Denied

Diemolding Corp. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1976 to 1996. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Diemolding Corp.

12 devices

1-12 of 12

Cleared Oct 10, 1996

THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK,...

K962749 · BWF

Anesthesiology · 87d

Cleared Jul 25, 1996

MEDSHIELD/AEROCHAMBER

K961455 · CCQ

Anesthesiology · 100d

Cleared Jul 25, 1990

ACCESS. KIT FOR THE BIOSURGE SYNCHRONOUS AUTOTRANS

K902713 · CAC

Anesthesiology · 35d

Cleared Jul 18, 1990

CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR

General Hospital · 5d

Cleared Jan 05, 1977

I.V. DRIP MONITOR ALARM DEVICE, MONIFLO

K760931 · FLN

General Hospital · 68d

FILTER, VACUUM LINE LINEGUARD

K760420 · KPQ

Radiology · 17d

Diemolding Corp. - FDA 510(k) Cleared Devices

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