FDA.report

510(k) K253281

Device
UpDoc
Applicant
Updoc, Inc.
510(k) number
K253281
Product code
NDC
Decision
Substantially Equivalent (SESE)
Decision date
2025-12-23
Date received
2025-09-29
Regulation
868.1890
Classification name
Calculator, Drug Dose
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Kendal Dinsmore
Address
851 Sierra Vista Ave., Unit A Mountain View CA US 94043 94043

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
00860015223906UpDocUpDoc Inc.2026-01-13

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