Medical Device Manufacturer · US , Walker , MI

Everest & Jennings, Inc. - FDA 510(k) Cleared Devices

30 submissions · 30 cleared · Since 1983

Total

Cleared

Denied

Everest & Jennings, Inc. has 30 FDA 510(k) cleared physical medicine devices. Based in Walker, US.

Historical record: 30 cleared submissions from 1983 to 1994.

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

Everest & Jennings, 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 - Everest & Jennings, Inc.

30 devices

1-12 of 30

Cleared Mar 28, 1994

KID POWER

K925865 · ITI

Physical Medicine · 494d

Cleared Feb 17, 1994

RECORD

K940303 · IOR

Physical Medicine · 24d

Cleared Feb 17, 1994

NITRO

K940304 · IOR

Physical Medicine · 24d

Cleared Mar 31, 1993

UNIVERSAL WHEELCHAIR

K930411 · IOR

Physical Medicine · 64d

Cleared Mar 31, 1993

PREMIER 2 WHEELCHAIR

K930412 · IOR

Physical Medicine · 64d

Cleared Mar 31, 1993

PREMIER CLASSIC

K930413 · IOR

Physical Medicine · 64d

Cleared Dec 17, 1991

SPECIALTY CONTROLS INTERFACE

K913645 · ITI

Physical Medicine · 123d

Cleared Nov 19, 1991

POWER RECLINER WHEELCHAIR

K914091 · ITI

Physical Medicine · 69d

Cleared Dec 21, 1990

ELLIPSE 2.3

K905621 · IOR

Physical Medicine · 7d

Cleared Nov 26, 1990

TEMPEST ELECTRIC WHEELCHAIR

K904958 · ITI

Physical Medicine · 21d

Cleared Nov 07, 1990

XCALIBER

K904818 · ITI

Physical Medicine · 14d

Cleared Nov 05, 1990

MAGNUM

K904817 · ITI

Physical Medicine · 12d

Everest & Jennings, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Everest & Jennings, Inc.

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