510(k) K182150
K182150 is an FDA 510(k) premarket notification submitted by Devon Medical Products (Jiangsu), Ltd. for the device "Devon 52 Sequential Compression Device". The FDA issued a decision of Substantially Equivalent on Dec 18, 2018. The device falls under product code JOW (Sleeve, Limb, Compressible), a Class II device regulated under 21 CFR 870.5800. Devon Medical Products (Jiangsu), Ltd. has 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 18, 2018
- Date Received
- Aug 8, 2018
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sleeve, Limb, Compressible
- Device Class
- Class II
- Regulation Number
- 870.5800
- Review Panel
- CV
- Submission Type
- 510(k)