Medical Device Manufacturer · US , Ronkonkoma , NY

Cybex - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1984

Official Website

Total

Cleared

Denied

Cybex has 9 FDA 510(k) cleared medical devices. Based in Ronkonkoma, US.

Historical record: 9 cleared submissions from 1984 to 1995. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Cybex Filter by specialty or product code using the sidebar.

Cybex 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 - Cybex

9 devices

1-9 of 9

Cleared Jun 21, 1995

CYBEX 770

K950095 · IKK

Physical Medicine · 162d

Cleared Feb 14, 1991

CYBEX 6000

K905525 · IKK

Physical Medicine · 66d

Cleared Apr 25, 1990

LINEAR LIFT DEVICE

K881676 · IKK

Physical Medicine · 736d

Cleared Apr 25, 1990

CYBEX BACK TESTING AND REHABILITATION SYSTEM

K881681 · IKK

Physical Medicine · 736d

Cleared Oct 24, 1989

METABOLIC SYSTEMS

K894154 · ISD

Physical Medicine · 132d

Physical Medicine · 62d

Cleared Feb 19, 1985

LINEAR LIFT DEVICE

K844368 · IKK

Physical Medicine · 98d

Cleared Nov 29, 1984

CYBEX TORSO TESTING & REHABILITATION

K843739 · IKK

Physical Medicine · 65d

Cybex - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Cybex

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