510(k) K172482
K172482 is an FDA 510(k) premarket notification submitted by Covidien for the device "The Nellcor pulse oximetry monitor interface cable". The FDA issued a decision of Substantially Equivalent on Dec 15, 2017. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Covidien has 224 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 15, 2017
- Date Received
- Aug 16, 2017
- 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)