Submission Details
| 510(k) Number | K920994 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 02, 1992 |
| Decision Date | May 15, 1992 |
| Days to Decision | 74 days |
| Submission Type | Traditional |
| Review Panel | Ear, Nose, Throat (EN) |
| Summary | Statement |
K920994 is an FDA 510(k) clearance for the HOOD NASAL SEPTAL BUTTON, a Button, Nasal Septal, submitted by Hood Laboratories (Pembroke, US). The FDA issued a Cleared decision on May 15, 1992, 74 days after receiving the submission on March 2, 1992. This device falls under the Ear, Nose, Throat review panel.
| 510(k) Number | K920994 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 02, 1992 |
| Decision Date | May 15, 1992 |
| Days to Decision | 74 days |
| Submission Type | Traditional |
| Review Panel | Ear, Nose, Throat (EN) |
| Summary | Statement |
| Product Code | LFB — Button, Nasal Septal |
| Device Class | — |