510(k) K951492
K951492 is an FDA 510(k) premarket notification submitted by United States Surgical, A Division of Tyco Healthc for the device "RIB RESECTOR". The FDA issued a decision of Substantially Equivalent on May 18, 1995. The device falls under product code HAO (Instrument, Surgical, Non-Powered), a Class I device regulated under 21 CFR 882.4535. United States Surgical, A Division of Tyco Healthc has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 18, 1995
- Date Received
- March 31, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Instrument, Surgical, Non-Powered
- Device Class
- Class I
- Regulation Number
- 882.4535
- Review Panel
- NE
- Submission Type