The following data is part of a premarket notification filed by V. Mueller O.v. Baxter Healthcare Corp. with the FDA for Scissor - 1.5mm Probe Point, Angled.
Device ID | K760792 |
510k Number | K760792 |
Device Name: | SCISSOR - 1.5MM PROBE POINT, ANGLED |
Classification | Instruments, Surgical, Cardiovascular |
Applicant | V. MUELLER O.V. BAXTER HEALTHCARE CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | DWS |
CFR Regulation Number | 870.4500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1976-10-07 |
Decision Date | 1976-11-11 |