The following data is part of a premarket notification filed by Birtcher Corp. with the FDA for Surgical Cauteries Models 775-11,12,13,31,32 & 33.
Device ID | K854814 |
510k Number | K854814 |
Device Name: | SURGICAL CAUTERIES MODELS 775-11,12,13,31,32 & 33 |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | BIRTCHER CORP. 4501 N. ARDEN DR. P.O. BOX 4399 El Monte, CA 91731 |
Contact | Donald L Emmons |
Correspondent | Donald L Emmons BIRTCHER CORP. 4501 N. ARDEN DR. P.O. BOX 4399 El Monte, CA 91731 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-12-03 |
Decision Date | 1986-01-13 |