The following data is part of a premarket notification filed by Zinnanti Surgical Instruments, Inc. with the FDA for Jesberg Esophagoscope.
| Device ID | K892259 |
| 510k Number | K892259 |
| Device Name: | JESBERG ESOPHAGOSCOPE |
| Classification | Esophagoscope (flexible Or Rigid) |
| Applicant | ZINNANTI SURGICAL INSTRUMENTS, INC. 21540-B PRAIRIE ST. Chatsworth, CA 91311 |
| Contact | Anthony Zinnanti |
| Correspondent | Anthony Zinnanti ZINNANTI SURGICAL INSTRUMENTS, INC. 21540-B PRAIRIE ST. Chatsworth, CA 91311 |
| Product Code | EOX |
| CFR Regulation Number | 874.4710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-04-04 |
| Decision Date | 1989-06-16 |