The following data is part of a premarket notification filed by Cameron-miller, Inc. with the FDA for Technicator.
Device ID | K812702 |
510k Number | K812702 |
Device Name: | TECHNICATOR |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | CAMERON-MILLER, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-09-23 |
Decision Date | 1981-11-05 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TECHNICATOR 72195330 0797824 Dead/Expired |
RESEARCH INSTITUTE OF AMERICA, INC., THE 1964-06-10 |