ClearanceBrief
Company ยท US

Diemolding Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1996. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BWFSpirometer, Therapeutic (Incentive)2
BSKCuff, Tracheal Tube, Inflatable1
BYPMouthpiece, Breathing1
BZAConnector, Airway (Extension)1
CACApparatus, Autotransfusion1
CANRegulator, Pressure, Gas Cylinder1
CBDBottle, Collection, Breathing System (Calibrated)1
CCQNebulizer, Medicinal, Non-Ventilatory (Atomizer)1
FLNMonitor, Electric For Gravity Flow Infusion Systems1
JDZMixer, Cement, For Clinical Use1
KPQSystem, Simulation, Radiation Therapy1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 10, 1996K962749THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK, RESISTOR/PORT/MOUTHPIECE, RESISTOR/PORT
Diemolding Corp.
BWF
Jul 25, 1996K961455MEDSHIELD/AEROCHAMBER
Diemolding Corp.
CCQ
Jul 25, 1990K902713ACCESS. KIT FOR THE BIOSURGE SYNCHRONOUS AUTOTRANS
Diemolding Corp.
CAC
Jul 18, 1990K902114CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR
Diemolding Corp.
BSK
Mar 15, 1990K900754RESPIREX 2
Diemolding Corp.
BWF
Jun 23, 1989K893791BREATHING MOUTHPIECE
Diemolding Corp.
BYP
Nov 27, 1978K781759RESCAL
Diemolding Corp.
BZA
Jul 27, 1978K780750O2 CONNECTOR
Diemolding Corp.
CAN
Mar 1, 1977K770369VACON TM
Diemolding Corp.
CBD
Jan 5, 1977K760931I.V. DRIP MONITOR ALARM DEVICE, MONIFLO
Diemolding Corp.
FLN
Oct 5, 1976K760636ORTHOMIX
Diemolding Corp.
JDZ
Aug 23, 1976K760420FILTER, VACUUM LINE LINEGUARD
Diemolding Corp.
KPQ

Latest recalls

DateFirm and productCodeLinked 510(k)
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