Atlas FDA

CYBEX 770

FDA 510(k) clearance K950095 · decided 1995-06-21

Clearance details

K-number
K950095
Device name
CYBEX 770
Applicant
Cybex
Decision
Substantially Equivalent
Date received
1995-01-10
Decision date
1995-06-21
Days to decision
162 days
Clearance type
Traditional
Product code
IKK
Device class
2
Regulation number
890.1925
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Ronkonkoma, NY, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
AMES THERAPY DEVICE (K123746)Ames Technology, Inc.2013-05-24
HUMAC SYSTEM (K952090)Computer Sports Medicine, Inc.1995-12-11
BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3AP (K951770)Biodex Medical Systems, Inc.1995-11-16
CC RIDER, MODEL ME180 (K951916)Mettler Electronics Corp.1995-10-04
MOTIVATOR FTR 2000 (K942229)Hogan & Hartson1995-02-27
DEXTER ISOKINETIC (K944732)Cedaron Medical, Inc.1995-02-03
THE BTE DYNAMIC LIFT (K924414)Baltimore Therapeutic Equipment Co.1993-02-12
CLOSED CHAIN ATTACHMENT, MODEL #820-520 (K923350)Biodan Medical Systems, Ltd.1992-07-23
TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR (K922772)Biodan Medical Systems, Ltd.1992-07-13
SINGLE CHAIR INTEGRAL BACK ATTACHMENT (K922092)Biodan Medical Systems, Ltd.1992-05-26
DEXTER HAND EVALUATION AND THERAPY SYSTEM (K915144)Cedars Medical Center1992-04-02
BIODEX SYSTEM 2 AUTOPROGRAM (K915846)Biodex Corp.1992-01-13

Recalls involving this device

No recalls on record reference this clearance.