FDA 510(k)

SUDO PATH

K-Number: K131568 · 2013-06-28

Decision Date2013-06-28

Product CodeGZO

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

SUDO PATH is the device name listed in this FDA 510(k) record. The listed applicant is Ld Technology, LLC. It received FDA 510(k) clearance on 2013-06-28 under 510(k) number K131568. The device is classified under product code GZO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUDO PATH?

SUDO PATH is a medical device that received FDA 510(k) clearance on 2013-06-28. The listed applicant is Ld Technology, LLC. The 510(k) number is K131568.

When did SUDO PATH receive FDA 510(k) clearance?

SUDO PATH received FDA 510(k) clearance on 2013-06-28, under 510(k) number K131568.

Who is the listed applicant for SUDO PATH?

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

What is the FDA product code for SUDO PATH?

The FDA product code for SUDO PATH is GZO.

Other records listing Ld Technology, LLC as applicant

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Related Devices (Code: GZO)

K111308ZYTO HAND CRADLEZyto Technologies, Inc.K102166ELECTRO INTERSTITIAL SCANLd Technology, LLC K100233SUDOSCANImpeto Medical K053004MSAS-VANTAGEBiomeridian, Int.K032935EPI-SCAN, MODEL P 100Edx Epi-Scan, Inc.K023355ASYRAGalloway Technologies, LLC

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.