510(k) K903205
K903205 is an FDA 510(k) premarket notification submitted by United States Surgical, A Division of Tyco Healthc for the device "AUTO SUTURE(R) ENDOSCOPIC CLAMP". The FDA issued a decision of Substantially Equivalent on October 11, 1990. The device falls under product code HDA (Forceps, Obstetrical), a Class II device regulated under 21 CFR 884.4400. 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
- October 11, 1990
- Date Received
- July 20, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Forceps, Obstetrical
- Device Class
- Class II
- Regulation Number
- 884.4400
- Review Panel
- OB
- Submission Type