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FDA 510(k)

UTAH ARTIFICAL ARM

K-Number: K802642 · 1980-11-12

ApplicantMotion Control, Inc.
Decision Date1980-11-12
Product CodeIRE
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

UTAH ARTIFICAL ARM is the device name listed in this FDA 510(k) record. The listed applicant is Motion Control, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802642. The device is classified under product code IRE. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UTAH ARTIFICAL ARM?

UTAH ARTIFICAL ARM is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Motion Control, Inc.. The 510(k) number is K802642.

When did UTAH ARTIFICAL ARM receive FDA 510(k) clearance?

UTAH ARTIFICAL ARM received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802642.

Who is the listed applicant for UTAH ARTIFICAL ARM?

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

What is the FDA product code for UTAH ARTIFICAL ARM?

The FDA product code for UTAH ARTIFICAL ARM is IRE.

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 Motion Control, 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.

K872040PHORESOR II (TM), MODEL PM700K862236MYOLAB II, MODEL ML-200K780310DERMATRON IONTOPHORESIS DEVICE

Related Devices (Code: IRE)

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.

K822632ELBOW PROSTHESISHosmer Dorrance Corp.

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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