Erich Jaeger, Inc.
Erich Jaeger, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 2000.
Top product codes for Erich Jaeger, Inc.
Recent clearances by Erich Jaeger, Inc.
- K000396 — APNOESCREEN PRO, ALPHA SCREEN PRO
- K972419 — TOENNIES NEUROSCREEN SYSTEM
- K960078 — ASTHMA MONITOR
- K932744 — FLOWSCREEN
- K933839 — MASTER SCREEN PNUEMO
- K853443 — ALVEO-DIFFUSION TEST
- K853390 — INFANT BODY TEST
- K853409 — SCREENMATE
- K853434 — ERGO-PNEUMOTEST
- K853360 — N20 TEST
- K852337 — PNEUMOSCOPE
- K843846 — UNIVERSAL-BODYTEST
- K843851 — BODYSCREEN II
- K843841 — ERGO-OXYSCREEN
- K843860 — OXYSCREEN
- K843843 — HE TEST
- K843850 — UNIVERSAL-ERGOTEST
- K843853 — LAUF-ERGOTEST
- K843855 — ERGOTEST 40 & 45
- K843859 — LAUF-ERGOTEST JUNIOR
- K843857 — TRANSFERSCREEN II
- K843848 — AW TEST
- K843852 — APTA-BRONCHOSCREEN
- K843849 — PNEUMOSCREEN
- K843840 — N2 TEST
- K843844 — CO2 TEST
- K843845 — CO TEST
- K843847 — O2 TEST
Data sourced from openFDA. This site is unofficial and independent of the FDA.