510(k) K033660
K033660 is an FDA 510(k) premarket notification submitted by Rudolf Storz GmbH for the device "STORZ RANEY SCALP CLIP, MODEL 1-20-004-05". The FDA issued a decision of Substantially Equivalent on January 7, 2004. The device falls under product code HBO (Clip, Scalp), a Class II device regulated under 21 CFR 882.4150.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 7, 2004
- Date Received
- November 21, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Clip, Scalp
- Device Class
- Class II
- Regulation Number
- 882.4150
- Review Panel
- NE
- Submission Type