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FDA 510(k)

MANUAL TOUCHE SYSTEM

K-Number: K022777 · 2002-11-19

ApplicantOnux Medical, Inc.
Decision Date2002-11-19
Product CodeGAQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MANUAL TOUCHE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Onux Medical, Inc.. It received FDA 510(k) clearance on 2002-11-19 under 510(k) number K022777. The device is classified under product code GAQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANUAL TOUCHE SYSTEM?

MANUAL TOUCHE SYSTEM is a medical device that received FDA 510(k) clearance on 2002-11-19. The listed applicant is Onux Medical, Inc.. The 510(k) number is K022777.

When did MANUAL TOUCHE SYSTEM receive FDA 510(k) clearance?

MANUAL TOUCHE SYSTEM received FDA 510(k) clearance on 2002-11-19, under 510(k) number K022777.

Who is the listed applicant for MANUAL TOUCHE SYSTEM?

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

What is the FDA product code for MANUAL TOUCHE SYSTEM?

The FDA product code for MANUAL TOUCHE SYSTEM is GAQ.

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Other records listing Onux Medical, 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.

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Related Devices (Code: GAQ)

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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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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