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Erich Jaeger, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
36
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K023120OXYCON MOBILENovember 12, 2003
K023796MS PAED-BABY BODYMarch 3, 2003
K021138SLEEPSCREEN/APNOESCREEN CARDIOFebruary 12, 2003
K000396APNOESCREEN PRO, ALPHA SCREEN PRODecember 27, 2000
K001502AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PROJuly 12, 2000
K000648SPIRO PROMarch 29, 2000
K992214OXYCON PROFebruary 22, 2000
K984465OXYCONALPHA WITH OPTION ECGOctober 27, 1999
K980094MODIFICATION TO THE OXYCONALPHAJuly 28, 1998
K972419TOENNIES NEUROSCREEN SYSTEMApril 30, 1998
K960078ASTHMA MONITORSeptember 20, 1996
K932744FLOWSCREENMarch 7, 1994
K933839MASTER SCREEN PNUEMOMarch 7, 1994
K853443ALVEO-DIFFUSION TESTFebruary 21, 1986
K853434ERGO-PNEUMOTESTFebruary 5, 1986
K853409SCREENMATEFebruary 5, 1986
K853390INFANT BODY TESTFebruary 5, 1986
K853360N20 TESTSeptember 3, 1985
K852337PNEUMOSCOPEJuly 1, 1985
K843846UNIVERSAL-BODYTESTFebruary 14, 1985