510(k) K193350
K193350 is an FDA 510(k) premarket notification submitted by Leadtek Research, Inc. for the device "Leadtek Fingertip Pulse Oximeter". The FDA issued a decision of Substantially Equivalent on Apr 27, 2020. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Leadtek Research, Inc. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 27, 2020
- Date Received
- Dec 3, 2019
- 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
- 510(k)