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FDA 510(k)

cCeLL - In vivo

K-Number: K233391 · 2024-08-21

ApplicantVPIX Medical, Inc.
Decision Date2024-08-21
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

cCeLL - In vivo is a medical device manufactured by VPIX Medical, Inc.. It received FDA 510(k) clearance on 2024-08-21 under approval number K233391. 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 cCeLL - In vivo?

cCeLL - In vivo is a medical device that received FDA 510(k) clearance on 2024-08-21. It is manufactured by VPIX Medical, Inc.. The 510(k) number is K233391.

When was cCeLL - In vivo approved by the FDA?

cCeLL - In vivo received FDA 510(k) clearance on 2024-08-21, under approval number K233391.

What company makes cCeLL - In vivo?

cCeLL - In vivo is manufactured by VPIX Medical, Inc..

What is the FDA product code for cCeLL - In vivo?

The FDA product code for cCeLL - In vivo is GWG.

Other Devices by VPIX Medical, Inc.

K251852cCeLL - In vivo with Drop-In Robo (CN100-2W2C488775, CN100-1W1C775, DR200)

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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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