UpDoc
by Updoc, Inc. 510(k)
Active
510(k) K253281
Overview
The UpDoc is a calculator device for drug dose calculations used in anesthesiology. It is designed to assist medical professionals in determining appropriate medication dosages for patients.
The UpDoc is supplied by Updoc, Inc. and is classified as a Class II medical device. It is not specified as single-use or reusable, and no information regarding sterility, MRI safety, or storage conditions is provided. The device has received FDA 510(k) clearance with product code NDC.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK253281 | Date23 Dec 2025 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- NDC
- Device Class
- Class II
- Regulation
- 21 CFR Part 868.1890
- Advisory Committee
- Anesthesiology
- FDA Decision
- SESE Substantially Equivalent
Other devices from Updoc, Inc.
Questions
What is the UpDoc device used for?
The UpDoc is a calculator device specifically designed for drug dose calculations in anesthesiology. It assists medical professionals in determining appropriate medication dosages for patients.
Is the UpDoc a single-use or reusable device?
The device is not specified as single-use or reusable in the provided information. Users should consult the manufacturer's instructions for specific guidance on usage and disposal.
What regulatory approvals does the UpDoc have?
The UpDoc has received FDA 510(k) clearance with product code NDC. It is classified as a Class II medical device and is substantially equivalent to other devices in this category.
How is the UpDoc supplied?
The UpDoc is supplied by Updoc, Inc. No information regarding sterility, MRI safety, or storage conditions is provided in the device data.