Erich Jaeger B.V.

FDA Regulatory Profile

Erich Jaeger B.V. appears in FDA public data with 0 recalls, 36 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Nov 12, 2003.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K023120OXYCON MOBILENov 12, 2003
K023796MS PAED-BABY BODYMar 3, 2003
K021138SLEEPSCREEN/APNOESCREEN CARDIOFeb 12, 2003
K000396APNOESCREEN PRO, ALPHA SCREEN PRODec 27, 2000
K001502AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PROJul 12, 2000
K000648SPIRO PROMar 29, 2000
K992214OXYCON PROFeb 22, 2000
K984465OXYCONALPHA WITH OPTION ECGOct 27, 1999
K980094MODIFICATION TO THE OXYCONALPHAJul 28, 1998
K972419TOENNIES NEUROSCREEN SYSTEMApr 30, 1998
K960078ASTHMA MONITORSep 20, 1996
K932744FLOWSCREENMar 7, 1994
K933839MASTER SCREEN PNUEMOMar 7, 1994
K853443ALVEO-DIFFUSION TESTFeb 21, 1986
K853409SCREENMATEFeb 5, 1986
K853434ERGO-PNEUMOTESTFeb 5, 1986
K853390INFANT BODY TESTFeb 5, 1986
K853360N20 TESTSep 3, 1985
K852337PNEUMOSCOPEJul 1, 1985
K843851BODYSCREEN IIFeb 14, 1985