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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 the device name listed in this FDA 510(k) record. The listed applicant is VPIX Medical, Inc.. It received FDA 510(k) clearance on 2024-08-21 under 510(k) 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. The listed applicant is VPIX Medical, Inc.. The 510(k) number is K233391.

When did cCeLL - In vivo receive FDA 510(k) clearance?

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

Who is the listed applicant for cCeLL - In vivo?

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

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

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

Other records listing VPIX Medical, Inc. 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.

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

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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