510(k) K090308
K090308 is an FDA 510(k) premarket notification submitted by Stortford Medical, LLC for the device "RESTEP DVY SYSTEM, MODEL RSP-101". The FDA issued a decision of Substantially Equivalent on May 1, 2009. The device falls under product code JOW (Sleeve, Limb, Compressible), a Class II device regulated under 21 CFR 870.5800. Stortford Medical, LLC has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 1, 2009
- Date Received
- Feb 6, 2009
- Clearance Type
- Traditional
- 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)