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FDA 510(k)

CYBEX BACK TESTING AND REHABILITATION SYSTEM

K-Number: K881681 · 1990-04-25

ApplicantCybex
Decision Date1990-04-25
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CYBEX BACK TESTING AND REHABILITATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cybex. It received FDA 510(k) clearance on 1990-04-25 under 510(k) number K881681. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYBEX BACK TESTING AND REHABILITATION SYSTEM?

CYBEX BACK TESTING AND REHABILITATION SYSTEM is a medical device that received FDA 510(k) clearance on 1990-04-25. The listed applicant is Cybex. The 510(k) number is K881681.

When did CYBEX BACK TESTING AND REHABILITATION SYSTEM receive FDA 510(k) clearance?

CYBEX BACK TESTING AND REHABILITATION SYSTEM received FDA 510(k) clearance on 1990-04-25, under 510(k) number K881681.

Who is the listed applicant for CYBEX BACK TESTING AND REHABILITATION SYSTEM?

The FDA 510(k) record lists Cybex as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CYBEX BACK TESTING AND REHABILITATION SYSTEM?

The FDA product code for CYBEX BACK TESTING AND REHABILITATION SYSTEM is IKK.

Related Clinical Trials

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Other records listing Cybex as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K950095CYBEX 770K905525CYBEX 6000K881676LINEAR LIFT DEVICEK894154METABOLIC SYSTEMSK873599EDI 320K872911CYBEX 340

View all 9 devices →

Related Devices (Code: IKK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K123746AMES THERAPY DEVICEAmes Technology, Inc.K952090HUMAC SYSTEMComputer Sports Medicine, Inc.K951770BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3APBiodex Medical Systems, Inc.K951916CC RIDER, MODEL ME180Mettler Electronics Corp.K950095CYBEX 770CybexK942229MOTIVATOR FTR 2000Hogan & Hartson

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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