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FDA 510(k)

TOUCHPACS SUITE

K-Number: K112008 · 2012-01-06

ApplicantTouch Medical Solutions, Inc.
Decision Date2012-01-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TOUCHPACS SUITE is the device name listed in this FDA 510(k) record. The listed applicant is Touch Medical Solutions, Inc.. It received FDA 510(k) clearance on 2012-01-06 under 510(k) number K112008. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOUCHPACS SUITE?

TOUCHPACS SUITE is a medical device that received FDA 510(k) clearance on 2012-01-06. The listed applicant is Touch Medical Solutions, Inc.. The 510(k) number is K112008.

When did TOUCHPACS SUITE receive FDA 510(k) clearance?

TOUCHPACS SUITE received FDA 510(k) clearance on 2012-01-06, under 510(k) number K112008.

Who is the listed applicant for TOUCHPACS SUITE?

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

What is the FDA product code for TOUCHPACS SUITE?

The FDA product code for TOUCHPACS SUITE is LLZ.

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Related Devices (Code: LLZ)

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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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