510(k) K041677
K041677 is an FDA 510(k) premarket notification submitted by Karma Medical Products Co., Ltd. for the device "KARMA SCOOTER, MODEL KS-747.2". The FDA issued a decision of Substantially Equivalent on Aug 5, 2004. The device falls under product code INI (Vehicle, Motorized 3-Wheeled), a Class II device regulated under 21 CFR 890.3800. Karma Medical Products Co., Ltd. has 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 5, 2004
- Date Received
- Jun 21, 2004
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Vehicle, Motorized 3-Wheeled
- Device Class
- Class II
- Regulation Number
- 890.3800
- Review Panel
- PM
- Submission Type
- 510(k)