The following data is part of a premarket notification filed by Smiths Industries Medical Systems, Inc. with the FDA for Berman Airway.
| Device ID | K936134 |
| 510k Number | K936134 |
| Device Name: | BERMAN AIRWAY |
| Classification | Airway, Oropharyngeal, Anesthesiology |
| Applicant | SMITHS INDUSTRIES MEDICAL SYSTEMS, INC. 15 KIT ST. Keene, NH 03431 |
| Contact | Timothy J Talcott |
| Correspondent | Timothy J Talcott SMITHS INDUSTRIES MEDICAL SYSTEMS, INC. 15 KIT ST. Keene, NH 03431 |
| Product Code | CAE |
| CFR Regulation Number | 868.5110 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-12-23 |
| Decision Date | 1994-01-28 |