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FDA 510(k)

NAUTILUS LEG EXTENSION TESTING & REHABILITATION

K-Number: K861206 · 1986-04-18

ApplicantNautilus Sports/Medical Industries, Inc.
Decision Date1986-04-18
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NAUTILUS LEG EXTENSION TESTING & REHABILITATION is the device name listed in this FDA 510(k) record. The listed applicant is Nautilus Sports/Medical Industries, Inc.. It received FDA 510(k) clearance on 1986-04-18 under 510(k) number K861206. 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 NAUTILUS LEG EXTENSION TESTING & REHABILITATION?

NAUTILUS LEG EXTENSION TESTING & REHABILITATION is a medical device that received FDA 510(k) clearance on 1986-04-18. The listed applicant is Nautilus Sports/Medical Industries, Inc.. The 510(k) number is K861206.

When did NAUTILUS LEG EXTENSION TESTING & REHABILITATION receive FDA 510(k) clearance?

NAUTILUS LEG EXTENSION TESTING & REHABILITATION received FDA 510(k) clearance on 1986-04-18, under 510(k) number K861206.

Who is the listed applicant for NAUTILUS LEG EXTENSION TESTING & REHABILITATION?

The FDA 510(k) record lists Nautilus Sports/Medical Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NAUTILUS LEG EXTENSION TESTING & REHABILITATION?

The FDA product code for NAUTILUS LEG EXTENSION TESTING & REHABILITATION is IKK.

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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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