510(k) K903205

AUTO SUTURE(R) ENDOSCOPIC CLAMP by United States Surgical, A Division of Tyco Healthc — Product Code HDA

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