510(k) K230277
K230277 is an FDA 510(k) premarket notification submitted by Cofoe Medical Technology Co., Ltd. for the device "Pulse Oximeter(Model OHT60,OXH78)". The FDA issued a decision of Substantially Equivalent on January 4, 2024. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 4, 2024
- Date Received
- February 1, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Oximeter
- Device Class
- Class II
- Regulation Number
- 870.2700
- Review Panel
- AN
- Submission Type