510(k) K023001
K023001 is an FDA 510(k) premarket notification submitted by Home Care Technology Co., Ltd. for the device "HOME CARE VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, HT-326L". The FDA issued a decision of Substantially Equivalent on Apr 8, 2003. The device falls under product code IPF (Stimulator, Muscle, Powered), a Class II device regulated under 21 CFR 890.5850. Home Care Technology Co., Ltd. has 3 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 8, 2003
- Date Received
- Sep 9, 2002
- 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
- 510(k)