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FDA 510(k)

BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM

K-Number: K883198 · 1988-10-24

Decision Date1988-10-24
Product CodeKHX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Mechanical Technology, Inc.. It received FDA 510(k) clearance on 1988-10-24 under 510(k) number K883198. The device is classified under product code KHX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM?

BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1988-10-24. The listed applicant is Advanced Mechanical Technology, Inc.. The 510(k) number is K883198.

When did BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM receive FDA 510(k) clearance?

BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM received FDA 510(k) clearance on 1988-10-24, under 510(k) number K883198.

Who is the listed applicant for BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM?

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

What is the FDA product code for BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM?

The FDA product code for BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM is KHX.

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.

Other records listing Advanced Mechanical Technology, 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.

Related Devices (Code: KHX)

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.

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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