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FDA 510(k)

EAV KINDLING 2000S GSR DEVICE

K-Number: K020564 · 2002-04-30

ApplicantVirbrant Health
Decision Date2002-04-30
Product CodeGZO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EAV KINDLING 2000S GSR DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Virbrant Health. It received FDA 510(k) clearance on 2002-04-30 under 510(k) number K020564. 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 EAV KINDLING 2000S GSR DEVICE?

EAV KINDLING 2000S GSR DEVICE is a medical device that received FDA 510(k) clearance on 2002-04-30. The listed applicant is Virbrant Health. The 510(k) number is K020564.

When did EAV KINDLING 2000S GSR DEVICE receive FDA 510(k) clearance?

EAV KINDLING 2000S GSR DEVICE received FDA 510(k) clearance on 2002-04-30, under 510(k) number K020564.

Who is the listed applicant for EAV KINDLING 2000S GSR DEVICE?

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

What is the FDA product code for EAV KINDLING 2000S GSR DEVICE?

The FDA product code for EAV KINDLING 2000S GSR DEVICE 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, 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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