UpDoc
K-Number: K253281 · 2025-12-23
ApplicantUpdoc, Inc.
Decision Date2025-12-23
Product CodeNDC
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
UpDoc is the device name listed in this FDA 510(k) record. The listed applicant is Updoc, Inc.. It received FDA 510(k) clearance on 2025-12-23 under 510(k) 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. The listed applicant is Updoc, Inc.. The 510(k) number is K253281.
When did UpDoc receive FDA 510(k) clearance?
UpDoc received FDA 510(k) clearance on 2025-12-23, under 510(k) number K253281.
Who is the listed applicant for UpDoc?
The FDA 510(k) record lists Updoc, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UpDoc?
The FDA product code for UpDoc is NDC.
Related Devices (Code: NDC)
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.
Official Source
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