The following data is part of a premarket notification filed by Pilling Co. with the FDA for Jesberg Esophagoscopes W/austinetic S S.
Device ID | K760652 |
510k Number | K760652 |
Device Name: | JESBERG ESOPHAGOSCOPES W/AUSTINETIC S S |
Classification | Esophagoscope (flexible Or Rigid) |
Applicant | PILLING CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | EOX |
CFR Regulation Number | 874.4710 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1976-09-15 |
Decision Date | 1976-12-16 |