The following data is part of a premarket notification filed by Fujinon, Inc. with the FDA for Modified Bronchoscope And Accessories.
| Device ID | K933433 |
| 510k Number | K933433 |
| Device Name: | MODIFIED BRONCHOSCOPE AND ACCESSORIES |
| Classification | Bronchoscope (flexible Or Rigid) |
| Applicant | FUJINON, INC. 399 PARK AVE. New York, NY 10022 -4689 |
| Contact | Gary A Adler |
| Correspondent | Gary A Adler FUJINON, INC. 399 PARK AVE. New York, NY 10022 -4689 |
| Product Code | EOQ |
| CFR Regulation Number | 874.4680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-07-14 |
| Decision Date | 1993-11-01 |