Medical Device Manufacturer · US , Rockford , IL

Erich Jaeger, Inc. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1984

Total

Cleared

Denied

Erich Jaeger, Inc. has 28 FDA 510(k) cleared anesthesiology devices. Based in Rockford, US.

Historical record: 28 cleared submissions from 1984 to 2000.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Erich Jaeger, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Erich Jaeger, Inc.

28 devices

1-12 of 28

Cleared Dec 27, 2000

APNOESCREEN PRO, ALPHA SCREEN PRO

K000396 · MNR

Anesthesiology · 324d

Cleared Apr 30, 1998

TOENNIES NEUROSCREEN SYSTEM

Anesthesiology · 259d

Cleared Mar 07, 1994

FLOWSCREEN

K932744 · BTY

Anesthesiology · 272d

Cleared Mar 07, 1994

MASTER SCREEN PNUEMO

K933839 · BTY

Anesthesiology · 214d

Cleared Feb 21, 1986

ALVEO-DIFFUSION TEST

K853443 · BZC

Anesthesiology · 189d

Cleared Feb 05, 1986

INFANT BODY TEST

K853390 · CCM

Anesthesiology · 176d

Cleared Feb 05, 1986

SCREENMATE

K853409 · BZG

Anesthesiology · 177d

Cleared Feb 05, 1986

ERGO-PNEUMOTEST

K853434 · BZL

Anesthesiology · 174d

Anesthesiology · 136d

Erich Jaeger, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Erich Jaeger, Inc.

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