Osi Medical Dolphin Stand-Alone Pulse Oximeter, Model 2100 and Digital Dolphin Optical Sensor, Clip-On Finger Probe, Mod
510(k) K002036
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK002036 | Date17 Apr 2001 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- DQA
- Models / Variants
- Device Class
- Class II
- Regulation
- 21 CFR Part 870.2700
- Advisory Committee
- Cardiovascular
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 21 Sep 2026
The Osi Medical Dolphin Stand-Alone Pulse Oximeter, Model 2100, is a device used for the continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate. It is used in conjunction with the Digital Dolphin Optical Sensor, a clip-on finger probe. The device provides a noninvasive method for monitoring oxygen saturation and pulse rate. The Digital Dolphin Optical Sensor is designed to be used with the stand-alone pulse oximeter.
The Osi Medical Dolphin Stand-Alone Pulse Oximeter, Model 2100, and Digital Dolphin Optical Sensor are supplied as a system for monitoring SpO2 and pulse rate. The device has received FDA 510(k) clearance, with the K number K002036. The device is a Class 2 medical device, and its use is intended for continuous monitoring of oxygen saturation and pulse rate in a clinical setting.