RecallHawk

Unimed Reusable Finger Clip SpO2 Sensors (U403-49R and U103-49R)

Unimed Medical Supplies, Inc.

Summary

Unimed Medical Supplies, Inc. received 510(k) clearance for Unimed Reusable Finger Clip SpO2 Sensors (U403-49R and U103-49R), a DQA device. Cleared on 2026-04-14.

Details

Source

510(k) Clearance

External ID

K260931

Action Date

2026-04-14

Status

Special

Category

device

Product Code

DQA

Product Description

Unimed Reusable Finger Clip SpO2 Sensors (U403-49R and U103-49R). Product code: DQA.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Unimed Medical Supplies, Inc. has received 12 total clearances in our database.

Unimed Medical Supplies, Inc. has 12 FDA actions in our database, including 12 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Unimed Medical Supplies, Inc. have FDA actions?

Unimed Medical Supplies, Inc. has 12 FDA actions in our database, including 0 recalls and 12 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K260931" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for device

Related Actions