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FDA 510(k)

TENDER TOUCH

K-Number: K121401 · 2013-05-01

ApplicantSometech Corporation
Decision Date2013-05-01
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TENDER TOUCH is the device name listed in this FDA 510(k) record. The listed applicant is Sometech Corporation. It received FDA 510(k) clearance on 2013-05-01 under 510(k) number K121401. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENDER TOUCH?

TENDER TOUCH is a medical device that received FDA 510(k) clearance on 2013-05-01. The listed applicant is Sometech Corporation. The 510(k) number is K121401.

When did TENDER TOUCH receive FDA 510(k) clearance?

TENDER TOUCH received FDA 510(k) clearance on 2013-05-01, under 510(k) number K121401.

Who is the listed applicant for TENDER TOUCH?

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

What is the FDA product code for TENDER TOUCH?

The FDA product code for TENDER TOUCH is ILY.

Related Clinical Trials

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Other records listing Sometech Corporation 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.

K024186X-VIEWK031436MEDISCOPE

Related Devices (Code: ILY)

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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