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FDA 510(k)

MOTIVATOR FTR 2000

K-Number: K942229 · 1995-02-27

ApplicantHogan & Hartson
Decision Date1995-02-27
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOTIVATOR FTR 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1995-02-27 under 510(k) number K942229. 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 MOTIVATOR FTR 2000?

MOTIVATOR FTR 2000 is a medical device that received FDA 510(k) clearance on 1995-02-27. The listed applicant is Hogan & Hartson. The 510(k) number is K942229.

When did MOTIVATOR FTR 2000 receive FDA 510(k) clearance?

MOTIVATOR FTR 2000 received FDA 510(k) clearance on 1995-02-27, under 510(k) number K942229.

Who is the listed applicant for MOTIVATOR FTR 2000?

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

What is the FDA product code for MOTIVATOR FTR 2000?

The FDA product code for MOTIVATOR FTR 2000 is IKK.

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Other records listing Hogan & Hartson 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.

K974168COOPERSURGICAL INFRARED COAGULATORK973849BIOABSORBABLE BANKART TACKK973162DUAL RADIATION TARGETING SYSTEM DRTS DRAPEK950169RIBOSOMAL P EIA TEST SYSTEMK942389TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVESK946217CARDIOLIPIN M EIA TEST 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 770CybexK944732DEXTER ISOKINETICCedaron Medical, Inc.

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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