510(k) K902873
K902873 is an FDA 510(k) premarket notification submitted by United States Surgical, A Division of Tyco Healthc for the device "NONABSORBABLE DACRON SURGICAL SUTURE*". The FDA issued a decision of SN on September 27, 1990. The device falls under product code GAS (Suture, Nonabsorbable, Synthetic, Polyester), a Class II device regulated under 21 CFR 878.5000. United States Surgical, A Division of Tyco Healthc has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- September 27, 1990
- Date Received
- June 29, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Suture, Nonabsorbable, Synthetic, Polyester
- Device Class
- Class II
- Regulation Number
- 878.5000
- Review Panel
- SU
- Submission Type