FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LINEAR LIFT DEVICE

K Number: K844368 · Decision Feb 19, 1985
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
60
Applicant Total
9
Review Days
98

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Basic Information

Device Name
LINEAR LIFT DEVICE
K Number
K844368
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.1925
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Cybex
Date Received
November 13, 1984
Decision Date
February 19, 1985
Product Code
IKK
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IKK System, Isokinetic Testing And Evaluation

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Other Clearances by Cybex

K Number Device Name
K950095 CYBEX 770
K905525 CYBEX 6000
K881676 LINEAR LIFT DEVICE
K881681 CYBEX BACK TESTING AND REHABILITATION SYSTEM
K894154 METABOLIC SYSTEMS
K873599 EDI 320
K872911 CYBEX 340
K843739 CYBEX TORSO TESTING & REHABILITATION