The following data is part of a premarket notification filed by Hood Laboratories with the FDA for Hood Nasal Septal Button.
| Device ID | K920994 |
| 510k Number | K920994 |
| Device Name: | HOOD NASAL SEPTAL BUTTON |
| Classification | Button, Nasal Septal |
| Applicant | HOOD LABORATORIES 575 WASHINGTON ST. Pembroke, MA 02359 |
| Contact | Lewis H Marten |
| Correspondent | Lewis H Marten HOOD LABORATORIES 575 WASHINGTON ST. Pembroke, MA 02359 |
| Product Code | LFB |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-03-02 |
| Decision Date | 1992-05-15 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00815347023571 | K920994 | 000 |
| 00815347023564 | K920994 | 000 |
| 00815347023557 | K920994 | 000 |
| 00815347023540 | K920994 | 000 |
| 00815347023533 | K920994 | 000 |
| 00815347023526 | K920994 | 000 |