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FDA 510(k)

ZYTO HAND CRADLE

K-Number: K111308 · 2011-08-30

ApplicantZyto Technologies, Inc.
Decision Date2011-08-30
Product CodeGZO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ZYTO HAND CRADLE is the device name listed in this FDA 510(k) record. The listed applicant is Zyto Technologies, Inc.. It received FDA 510(k) clearance on 2011-08-30 under 510(k) number K111308. 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 ZYTO HAND CRADLE?

ZYTO HAND CRADLE is a medical device that received FDA 510(k) clearance on 2011-08-30. The listed applicant is Zyto Technologies, Inc.. The 510(k) number is K111308.

When did ZYTO HAND CRADLE receive FDA 510(k) clearance?

ZYTO HAND CRADLE received FDA 510(k) clearance on 2011-08-30, under 510(k) number K111308.

Who is the listed applicant for ZYTO HAND CRADLE?

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

What is the FDA product code for ZYTO HAND CRADLE?

The FDA product code for ZYTO HAND CRADLE is GZO.

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Related Devices (Code: GZO)

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.

K131568SUDO PATHLd Technology, LLCK102166ELECTRO INTERSTITIAL SCANLd Technology, LLCK100233SUDOSCANImpeto MedicalK053004MSAS-VANTAGEBiomeridian, Int.K032935EPI-SCAN, MODEL P 100Edx Epi-Scan, Inc.K023355ASYRAGalloway Technologies, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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