The following data is part of a premarket notification filed by Berchtold Holding Gmbh with the FDA for Hirsch Bipolar Coagulation Forceps And Adaptor Cables.
Device ID | K942319 |
510k Number | K942319 |
Device Name: | HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | BERCHTOLD HOLDING GMBH LUDWIGSTALER STR. 25 Tuttlingen, DE D-78532 |
Contact | David N Bulman |
Correspondent | David N Bulman BERCHTOLD HOLDING GMBH LUDWIGSTALER STR. 25 Tuttlingen, DE D-78532 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-05-13 |
Decision Date | 1994-06-08 |