The following data is part of a premarket notification filed by Sheridan Catheter Corp. with the FDA for Tracheal/bronchial Differential Ventilation Tube.
| Device ID | K851856 |
| 510k Number | K851856 |
| Device Name: | TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE |
| Classification | Tube, Tracheal/bronchial, Differential Ventilation (w/wo Connector) |
| Applicant | SHERIDAN CATHETER CORP. ROUTE 40 Argyle, NY 12809 |
| Contact | John S Steen |
| Correspondent | John S Steen SHERIDAN CATHETER CORP. ROUTE 40 Argyle, NY 12809 |
| Product Code | CBI |
| CFR Regulation Number | 868.5740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-04-26 |
| Decision Date | 1985-05-23 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 44026704617478 | K851856 | 000 |
| 34026704760146 | K851856 | 000 |
| 24026704397642 | K851856 | 000 |
| 24026704397659 | K851856 | 000 |
| 24026704397666 | K851856 | 000 |
| 24026704397673 | K851856 | 000 |
| 44026704397684 | K851856 | 000 |
| 34026704617433 | K851856 | 000 |
| 44026704617447 | K851856 | 000 |
| 34026704617457 | K851856 | 000 |
| 34026704617464 | K851856 | 000 |
| 34026704760085 | K851856 | 000 |