510(k) K904578

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

K904578 is an FDA 510(k) premarket notification submitted by United States Surgical, A Division of Tyco Healthc for the device "MODIFICATION AUTO SUTURE(R) ENDOSCOPIC CLAMP". The FDA issued a decision of Substantially Equivalent on October 30, 1990. The device falls under product code GET (Motor, Surgical Instrument, Pneumatic Powered), a Class I device regulated under 21 CFR 878.4820. 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 30, 1990
Date Received
October 2, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Motor, Surgical Instrument, Pneumatic Powered
Device Class
Class I
Regulation Number
878.4820
Review Panel
SU
Submission Type