The following data is part of a premarket notification filed by United States Surgical, A Division Of Tyco Healthc with the FDA for Auto Suture Endoscopic Suction/irrigatrion Device.
Device ID | K903207 |
510k Number | K903207 |
Device Name: | AUTO SUTURE ENDOSCOPIC SUCTION/IRRIGATRION DEVICE |
Classification | Laparoscope, Gynecologic (and Accessories) |
Applicant | UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
Contact | Steve Reitzler |
Correspondent | Steve Reitzler UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
Product Code | HET |
CFR Regulation Number | 884.1720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-07-20 |
Decision Date | 1990-09-25 |