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FDA 510(k)

PHAZX VLD-100

K-Number: K992129 · 1999-09-17

ApplicantPhazx Systems, Inc.
Decision Date1999-09-17
Product CodeGZO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PHAZX VLD-100 is the device name listed in this FDA 510(k) record. The listed applicant is Phazx Systems, Inc.. It received FDA 510(k) clearance on 1999-09-17 under 510(k) number K992129. 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 PHAZX VLD-100?

PHAZX VLD-100 is a medical device that received FDA 510(k) clearance on 1999-09-17. The listed applicant is Phazx Systems, Inc.. The 510(k) number is K992129.

When did PHAZX VLD-100 receive FDA 510(k) clearance?

PHAZX VLD-100 received FDA 510(k) clearance on 1999-09-17, under 510(k) number K992129.

Who is the listed applicant for PHAZX VLD-100?

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

What is the FDA product code for PHAZX VLD-100?

The FDA product code for PHAZX VLD-100 is GZO.

Related Clinical Trials

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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, LLCK111308ZYTO HAND CRADLEZyto Technologies, Inc.K102166ELECTRO INTERSTITIAL SCANLd Technology, LLCK100233SUDOSCANImpeto MedicalK053004MSAS-VANTAGEBiomeridian, Int.K032935EPI-SCAN, MODEL P 100Edx Epi-Scan, Inc.

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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