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FDA 510(k)

CYBEX 340

K-Number: K872911 · 1987-09-24

ApplicantCybex
Decision Date1987-09-24
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CYBEX 340 is the device name listed in this FDA 510(k) record. The listed applicant is Cybex. It received FDA 510(k) clearance on 1987-09-24 under 510(k) number K872911. 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 340?

CYBEX 340 is a medical device that received FDA 510(k) clearance on 1987-09-24. The listed applicant is Cybex. The 510(k) number is K872911.

When did CYBEX 340 receive FDA 510(k) clearance?

CYBEX 340 received FDA 510(k) clearance on 1987-09-24, under 510(k) number K872911.

Who is the listed applicant for CYBEX 340?

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 340?

The FDA product code for CYBEX 340 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 DEVICEK881681CYBEX BACK TESTING AND REHABILITATION SYSTEMK894154METABOLIC SYSTEMSK873599EDI 320

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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