510(k) K954334
K954334 is an FDA 510(k) premarket notification submitted by S.H.P. Intl. Pty., Ltd. for the device "ACUPLUS". The FDA issued a decision of Substantially Equivalent on January 22, 1996. The device falls under product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief), a Class II device regulated under 21 CFR 882.5890. S.H.P. Intl. Pty., Ltd. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 22, 1996
- Date Received
- September 18, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Nerve, Transcutaneous, For Pain Relief
- Device Class
- Class II
- Regulation Number
- 882.5890
- Review Panel
- NE
- Submission Type