510(k) K170965
K170965 is an FDA 510(k) premarket notification submitted by Shenzhen Jumper Medical Equipment Co., Ltd. for the device "Fingertip Pulse Oximeter". The FDA issued a decision of Substantially Equivalent on November 3, 2017. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Shenzhen Jumper Medical Equipment Co., Ltd. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 3, 2017
- Date Received
- March 31, 2017
- Clearance Type
- Special
- 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