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Intertech Resources, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
29
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K9613181ST RESPONSE DISPOSABLE MANOMETERDecember 17, 1996
K955008HEAT & MOISTURE EXCHANGERJanuary 30, 1996
K953580HEAT MOISTURE EXCHANGERSeptember 15, 1995
K952223XENON GAS BREATHING CIRCUITAugust 11, 1995
K952214SIMS INTERTECH HYPERINFLATION BAG SYSTEMJune 8, 1995
K952169SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRICJune 8, 1995
K952062PFT FILTERJune 8, 1995
K935036HEPA FILTERED HEAT AND MOISTURE EXCHANGERJanuary 25, 1994
K930816HEPA FILTERED HMEJuly 1, 1993
K922479DISPOSABLE ANESTHESIA BREATHING CIRCUIT, MODIFIEDOctober 30, 1992
K921624DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITSJune 30, 1992
K912504DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIEDOctober 23, 1991
K912065DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIEDOctober 23, 1991
K911328UNIVERSAL VOLUME VENTILATOR CIRCUIT, MODIFICATIONAugust 15, 1991
K911298PRESSURE LIMITING ELBOW WITH MANOMETER PORTJune 25, 1991
K910509PATIENT GAS SAMPLING LINE FOR OHMEDA 6000April 17, 1991
K903519INTERTECH(TM) HEAT AND MOISTURE EXCHANGERDecember 13, 1990
K9027331ST RESPONSE (TM) INFANT MANUAL RESUSCITATORAugust 22, 1990
K9005771ST RESPONSE REUSABLE MANUAL RESUSCITATOR (ADULT)July 16, 1990
K896923INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KITMarch 12, 1990