510(k) K882036
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 27, 1988
- Date Received
- May 16, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Guide, Needle, Surgical
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type