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FDA 510(k)

BIODEX BACK SYSTEM ATTACHMENT

K-Number: K900741 · 1990-02-26

ApplicantBiodex Corp.
Decision Date1990-02-26
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BIODEX BACK SYSTEM ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Biodex Corp.. It received FDA 510(k) clearance on 1990-02-26 under 510(k) number K900741. 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 BIODEX BACK SYSTEM ATTACHMENT?

BIODEX BACK SYSTEM ATTACHMENT is a medical device that received FDA 510(k) clearance on 1990-02-26. The listed applicant is Biodex Corp.. The 510(k) number is K900741.

When did BIODEX BACK SYSTEM ATTACHMENT receive FDA 510(k) clearance?

BIODEX BACK SYSTEM ATTACHMENT received FDA 510(k) clearance on 1990-02-26, under 510(k) number K900741.

Who is the listed applicant for BIODEX BACK SYSTEM ATTACHMENT?

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

What is the FDA product code for BIODEX BACK SYSTEM ATTACHMENT?

The FDA product code for BIODEX BACK SYSTEM ATTACHMENT is IKK.

Related Clinical Trials

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.

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Other records listing Biodex Corp. 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.

K915846BIODEX SYSTEM 2 AUTOPROGRAMK915648BIODEX SYSTEM 2 AUTOPROGRAMK913020BIODEX SYSTEM 2,MODEL S2-SK913021BIODEX,MODEL B-2000K900450BIODEX LIFT SIMULATORK860821BIODEX SYSTEM

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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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