510(k) K050921
K050921 is an FDA 510(k) premarket notification submitted by Easy Med Instrument Co., Ltd. for the device "EASYSTIM NMS-28". The FDA issued a decision of Substantially Equivalent on December 12, 2005. The device falls under product code IPF (Stimulator, Muscle, Powered), a Class II device regulated under 21 CFR 890.5850. Easy Med Instrument Co., Ltd. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 12, 2005
- Date Received
- April 13, 2005
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Muscle, Powered
- Device Class
- Class II
- Regulation Number
- 890.5850
- Review Panel
- PM
- Submission Type