FDA 510(k)

VIVA EB

K-Number: K120334 · 2012-06-08

Decision Date2012-06-08

Product CodeCBI

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

VIVA EB is the device name listed in this FDA 510(k) record. The listed applicant is Etview , Ltd.. It received FDA 510(k) clearance on 2012-06-08 under 510(k) number K120334. The device is classified under product code CBI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIVA EB?

VIVA EB is a medical device that received FDA 510(k) clearance on 2012-06-08. The listed applicant is Etview , Ltd.. The 510(k) number is K120334.

When did VIVA EB receive FDA 510(k) clearance?

VIVA EB received FDA 510(k) clearance on 2012-06-08, under 510(k) number K120334.

Who is the listed applicant for VIVA EB?

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

What is the FDA product code for VIVA EB?

The FDA product code for VIVA EB is CBI.

Other records listing Etview , Ltd. as applicant

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.

K181880VivaSight-SL (TVT) system K181886VivaSight-DL System K152438ETView VivaSight-SL (TVT) system K123853VIVASIGHT-DL SYSTEM K121028ETVIEW TRACHEOSCOPIC VENTILATION TUBE (TVT(TM))K113576DOUBLE LUMEN VIDEO TRACHEOSDOPE (DLVT) SYSTEM

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Related Devices (Code: CBI)

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.