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FDA 510(k)

UpDoc

K-Number: K253281 · 2025-12-23

ApplicantUpdoc, Inc.
Decision Date2025-12-23
Product CodeNDC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UpDoc is a medical device manufactured by Updoc, Inc.. It received FDA 510(k) clearance on 2025-12-23 under approval number K253281. The device is classified under product code NDC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UpDoc?

UpDoc is a medical device that received FDA 510(k) clearance on 2025-12-23. It is manufactured by Updoc, Inc.. The 510(k) number is K253281.

When was UpDoc approved by the FDA?

UpDoc received FDA 510(k) clearance on 2025-12-23, under approval number K253281.

What company makes UpDoc?

UpDoc is manufactured by Updoc, Inc..

What is the FDA product code for UpDoc?

The FDA product code for UpDoc is NDC.

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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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