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FDA 510(k)

CONVIVO

K-Number: K181116 · 2018-10-25

ApplicantCarl Zeiss Meditec, AG
Decision Date2018-10-25
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CONVIVO is a medical device manufactured by Carl Zeiss Meditec, AG. It received FDA 510(k) clearance on 2018-10-25 under approval number K181116. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVIVO?

CONVIVO is a medical device that received FDA 510(k) clearance on 2018-10-25. It is manufactured by Carl Zeiss Meditec, AG. The 510(k) number is K181116.

When was CONVIVO approved by the FDA?

CONVIVO received FDA 510(k) clearance on 2018-10-25, under approval number K181116.

What company makes CONVIVO?

CONVIVO is manufactured by Carl Zeiss Meditec, AG.

What is the FDA product code for CONVIVO?

The FDA product code for CONVIVO is GWG.

Other Devices by Carl Zeiss Meditec, AG

K162568INTRABEAM 600 K170667QEVO System with KINEVO 900 K162991YELLOW 560 Fluorescence Module K170638Retina Workplace K162684SL 220 K170171IOLMaster 700

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Related Devices (Code: GWG)

K161112KARL STORZ Flexible Video-Neuro-Endoscope SystemKARL STORZ Endoscopy-America, Inc. K152699Apollo SystemPenumbra, Inc. K170667QEVO System with KINEVO 900Carl Zeiss Meditec, AG K171332Artemis Neuro Evacuation DevicePenumbra, Inc. K170462KARL STORZ ShuntScopeKARL STORZ Endoscopy-America, Inc. K162880TIPCAM 1S 3D SystemKarl Storz Endoscopy America, 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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