The following data is part of a premarket notification filed by Guenter Bissinger Medizintechnik Gmbh with the FDA for Bissinger Cables, Cat. No. 801000xx.
Device ID | K981919 |
510k Number | K981919 |
Device Name: | BISSINGER CABLES, CAT. NO. 801000XX |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | GUENTER BISSINGER MEDIZINTECHNIK GMBH GOTTLIEB-DAIMLER-STR. 5 (ROHRLACHE) Teningen, DE D-79331 |
Contact | Dagmar S Maser |
Correspondent | Dagmar S Maser GUENTER BISSINGER MEDIZINTECHNIK GMBH GOTTLIEB-DAIMLER-STR. 5 (ROHRLACHE) Teningen, DE D-79331 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-06-01 |
Decision Date | 1998-08-06 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
M274615296B1 | K981919 | 000 |
04250676738868 | K981919 | 000 |
04250676738851 | K981919 | 000 |
04250676737908 | K981919 | 000 |
04250676736949 | K981919 | 000 |
04250676736932 | K981919 | 000 |
04250676736925 | K981919 | 000 |
04250676736918 | K981919 | 000 |
04250676736901 | K981919 | 000 |
04250676736895 | K981919 | 000 |
04250676736888 | K981919 | 000 |
04250676736871 | K981919 | 000 |
04250676736864 | K981919 | 000 |
04250676736857 | K981919 | 000 |
04250676736840 | K981919 | 000 |
04250676736833 | K981919 | 000 |
04250676738875 | K981919 | 000 |
04250676738882 | K981919 | 000 |
M274NRBC1181 | K981919 | 000 |
M2746152951 | K981919 | 000 |
M2742851991 | K981919 | 000 |
H834PM94501 | K981919 | 000 |
M274P94501 | K981919 | 000 |
04250676738981 | K981919 | 000 |
04250676738974 | K981919 | 000 |
04250676738967 | K981919 | 000 |
04250676738950 | K981919 | 000 |
04250676738943 | K981919 | 000 |
04250676738936 | K981919 | 000 |
04250676738929 | K981919 | 000 |
04250676738912 | K981919 | 000 |
04250676738905 | K981919 | 000 |
04250676738899 | K981919 | 000 |
04250676736826 | K981919 | 000 |