Diemolding Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K962749THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK, RESISTOR/PORT/MOUTHPIECE, RESISOctober 10, 1996
K961455MEDSHIELD/AEROCHAMBERJuly 25, 1996
K902713ACCESS. KIT FOR THE BIOSURGE SYNCHRONOUS AUTOTRANSJuly 25, 1990
K902114CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITORJuly 18, 1990
K900754RESPIREX 2March 15, 1990
K893791BREATHING MOUTHPIECEJune 23, 1989
K781759RESCALNovember 27, 1978
K780750O2 CONNECTORJuly 27, 1978
K770369VACON TMMarch 1, 1977
K760931I.V. DRIP MONITOR ALARM DEVICE, MONIFLOJanuary 5, 1977
K760636ORTHOMIXOctober 5, 1976
K760420FILTER, VACUUM LINE LINEGUARDAugust 23, 1976