510(k) K993758
K993758 is an FDA 510(k) premarket notification submitted by Medical Compression Systems (Dbn) , Ltd. for the device "PROAIR 3000 COMPRESSION SYSTEM". The FDA issued a decision of Substantially Equivalent on May 19, 2000. The device falls under product code JOW (Sleeve, Limb, Compressible), a Class II device regulated under 21 CFR 870.5800. Medical Compression Systems (Dbn) , Ltd. has 9 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 19, 2000
- Date Received
- Nov 5, 1999
- 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)