The following data is part of a premarket notification filed by United States Surgical, A Division Of Tyco Healthc with the FDA for Surgical Stapling Instru., Auto, Suture.
Device ID | K771177 |
510k Number | K771177 |
Device Name: | SURGICAL STAPLING INSTRU., AUTO, SUTURE |
Classification | Stapler, Surgical |
Applicant | UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | GAG |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1977-06-30 |
Decision Date | 1977-10-18 |