ClearanceBrief
Company ยท US

Cybex

FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1995. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IKKSystem, Isokinetic Testing And Evaluation7
ISDExerciser, Measuring1
KQXGoniometer, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 21, 1995K950095CYBEX 770
Cybex
IKK
Feb 14, 1991K905525CYBEX 6000
Cybex
IKK
Apr 25, 1990K881681CYBEX BACK TESTING AND REHABILITATION SYSTEM
Cybex
IKK
Apr 25, 1990K881676LINEAR LIFT DEVICE
Cybex
IKK
Oct 24, 1989K894154METABOLIC SYSTEMS
Cybex
ISD
Oct 16, 1987K873599EDI 320
Cybex
KQX
Sep 24, 1987K872911CYBEX 340
Cybex
IKK
Feb 19, 1985K844368LINEAR LIFT DEVICE
Cybex
IKK
Nov 29, 1984K843739CYBEX TORSO TESTING & REHABILITATION
Cybex
IKK

Latest recalls

DateFirm and productCodeLinked 510(k)
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