510(k) K203383
K203383 is an FDA 510(k) premarket notification submitted by Philips Consumer Lifestyle - Innovation Site Eindhoven for the device "Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62". The FDA issued a decision of Substantially Equivalent on Dec 15, 2020. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Philips Consumer Lifestyle - Innovation Site Eindhoven has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 15, 2020
- Date Received
- Nov 17, 2020
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pump, Breast, Powered
- Device Class
- Class II
- Regulation Number
- 884.5160
- Review Panel
- OB
- Submission Type
- 510(k)