510(k) K173565
K173565 is an FDA 510(k) premarket notification submitted by Jk-Holding GmbH for the device "Sunrise 6200, Sunrise 7200". The FDA issued a decision of Substantially Equivalent on Feb 14, 2018. The device falls under product code LEJ (Booth, Sun Tan), a Class II device regulated under 21 CFR 878.4635. Jk-Holding GmbH has 3 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 14, 2018
- Date Received
- Nov 17, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Booth, Sun Tan
- Device Class
- Class II
- Regulation Number
- 878.4635
- Review Panel
- SU
- Submission Type
- 510(k)