510(k) K051135
K051135 is an FDA 510(k) premarket notification submitted by Axiom Worldwide, Inc. for the device "AXIOM NVP8500". The FDA issued a decision of Substantially Equivalent on August 11, 2005. The device falls under product code IPF (Stimulator, Muscle, Powered), a Class II device regulated under 21 CFR 890.5850. Axiom Worldwide, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 11, 2005
- Date Received
- May 3, 2005
- Clearance Type
- Traditional
- 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