Medical Device Manufacturer · US , Walker , MI

Huntleigh Technology, Inc. - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 1981

Total

Cleared

Denied

Huntleigh Technology, Inc. has 23 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 23 cleared submissions from 1981 to 1999.

Browse the FDA 510(k) cleared devices submitted by Huntleigh Technology, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Huntleigh Technology, Inc.

23 devices

1-12 of 23

Cleared Nov 10, 1999

AKRON ATP9 TRACTION MACHINE

K992733 · ITH

Physical Medicine · 89d

Cleared Feb 21, 1997

RHEO DOPPLEX II (RD 2)

FLOWPLUS AC330 PUMP GARMENTS

K910188 · JOW

Cardiovascular · 132d

HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140

K900618 · KNG

Obstetrics & Gynecology · 76d

Cleared Mar 29, 1989

HUNTLEIGH DYNAMIC FLOTATION SYSTEM

K890012 · FNM

General Hospital · 85d

FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT

K881632 · JOW

Cardiovascular · 165d

Cleared Sep 23, 1988

FLOWTRON AC200/2

K874688 · IRP

Physical Medicine · 315d

Cleared Aug 10, 1988

HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5

K882644 · FNM

General Hospital · 44d

Cleared Sep 15, 1987

HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR.

K871271 · DRM

Cardiovascular · 168d

Huntleigh Technology, Inc. - FDA 510(k) Cleared Devices

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