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.

Diemolding Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

FDA 510(k) Regulatory Record - Diemolding Corp.

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