FDA 510(k)

SAFETOUCH

K-Number: K022861 · 2002-11-26

Decision Date2002-11-26

Product CodeNHM

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

SAFETOUCH is the device name listed in this FDA 510(k) record. The listed applicant is Rusin Medical Devices. It received FDA 510(k) clearance on 2002-11-26 under 510(k) number K022861. The device is classified under product code NHM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFETOUCH?

SAFETOUCH is a medical device that received FDA 510(k) clearance on 2002-11-26. The listed applicant is Rusin Medical Devices. The 510(k) number is K022861.

When did SAFETOUCH receive FDA 510(k) clearance?

SAFETOUCH received FDA 510(k) clearance on 2002-11-26, under 510(k) number K022861.

Who is the listed applicant for SAFETOUCH?

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

What is the FDA product code for SAFETOUCH?

The FDA product code for SAFETOUCH is NHM.

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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Related Devices (Code: NHM)

K014300SAFETOUCHJames D Rusin MD, MBA

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.