The following data is part of a premarket notification filed by Instrumentation Industries, Inc. with the FDA for Be 410 Endotracheal Tube/trach Tube, Pilot Repair.
| Device ID | K884638 |
| 510k Number | K884638 |
| Device Name: | BE 410 ENDOTRACHEAL TUBE/TRACH TUBE, PILOT REPAIR |
| Classification | Cuff, Tracheal Tube, Inflatable |
| Applicant | INSTRUMENTATION INDUSTRIES, INC. 2990 INDUSTRIAL BLVD. Bethel Park, PA 15102 |
| Contact | Clyde T Marrangoni |
| Correspondent | Clyde T Marrangoni INSTRUMENTATION INDUSTRIES, INC. 2990 INDUSTRIAL BLVD. Bethel Park, PA 15102 |
| Product Code | BSK |
| CFR Regulation Number | 868.5750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-11-07 |
| Decision Date | 1988-11-23 |