510(k) K993785
K993785 is an FDA 510(k) premarket notification submitted by Inrad for the device "ULTRACLIP TISSUE MARKER". The FDA issued a decision of Substantially Equivalent on February 4, 2000. The device falls under product code GDW (Staple, Implantable), a Class II device regulated under 21 CFR 878.4750. Inrad has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 4, 2000
- Date Received
- November 8, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Staple, Implantable
- Device Class
- Class II
- Regulation Number
- 878.4750
- Review Panel
- SU
- Submission Type