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FDA 510(k)

MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO

K-Number: K873659 · 1988-04-21

ApplicantUniversal Gym Equipment, Inc.
Decision Date1988-04-21
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO is the device name listed in this FDA 510(k) record. The listed applicant is Universal Gym Equipment, Inc.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K873659. 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 MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO?

MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Universal Gym Equipment, Inc.. The 510(k) number is K873659.

When did MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO receive FDA 510(k) clearance?

MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO received FDA 510(k) clearance on 1988-04-21, under 510(k) number K873659.

Who is the listed applicant for MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO?

The FDA 510(k) record lists Universal Gym Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO?

The FDA product code for MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO 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 Universal Gym Equipment, Inc. 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.

K873658ANKLE REFLEX TREATMENT UNIT (ARTU)

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

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

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