510(k) K854390
K854390 is an FDA 510(k) premarket notification submitted by Med-Tool, Inc. for the device "WIRE CUTTING PLIERS OR LINEMAN'S PLIERS". The FDA issued a decision of Substantially Equivalent on November 19, 1985. The device falls under product code HTC (Pliers, Surgical), a Class I device regulated under 21 CFR 878.4800. Med-Tool, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 19, 1985
- Date Received
- October 31, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pliers, Surgical
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type