The following data is part of a premarket notification filed by Sherwood Medical Industries with the FDA for Airway, Argyle Nasopharyngeal.
| Device ID | K760125 |
| 510k Number | K760125 |
| Device Name: | AIRWAY, ARGYLE NASOPHARYNGEAL |
| Classification | Airway, Nasopharyngeal |
| Applicant | SHERWOOD MEDICAL INDUSTRIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BTQ |
| CFR Regulation Number | 868.5100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-06-28 |
| Decision Date | 1976-07-19 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 40884521133137 | K760125 | 000 |
| 20884521815879 | K760125 | 000 |
| 30884521815869 | K760125 | 000 |
| 30884521133086 | K760125 | 000 |
| 30884521133109 | K760125 | 000 |
| 30884521133116 | K760125 | 000 |
| 20884521133126 | K760125 | 000 |
| 30884521133130 | K760125 | 000 |
| 20884521815831 | K760125 | 000 |
| 20884521815848 | K760125 | 000 |
| 30884521815883 | K760125 | 000 |
| 30884521133079 | K760125 | 000 |
| 40884521133076 | K760125 | 000 |
| 40884521133083 | K760125 | 000 |
| 50884521133103 | K760125 | 000 |
| 50884521133110 | K760125 | 000 |
| 40884521133120 | K760125 | 000 |
| 30884521815852 | K760125 | 000 |