The following data is part of a premarket notification filed by Warren C. Miller with the FDA for The Miller Nebulizer System.
| Device ID | K926055 |
| 510k Number | K926055 |
| Device Name: | THE MILLER NEBULIZER SYSTEM |
| Classification | Nebulizer (direct Patient Interface) |
| Applicant | WARREN C. MILLER 405 BLOSSOM ST. SUITE B Houston, TX 77055 |
| Contact | Charles S Boyd |
| Correspondent | Charles S Boyd WARREN C. MILLER 405 BLOSSOM ST. SUITE B Houston, TX 77055 |
| Product Code | CAF |
| CFR Regulation Number | 868.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-11-05 |
| Decision Date | 1993-02-03 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10709078000864 | K926055 | 000 |
| 10709078000833 | K926055 | 000 |
| 10709078009133 | K926055 | 000 |
| 10709078009140 | K926055 | 000 |
| 20612479203352 | K926055 | 000 |
| 20612479203376 | K926055 | 000 |
| 20612479203390 | K926055 | 000 |
| 20612479203413 | K926055 | 000 |
| 20612479203437 | K926055 | 000 |
| 10709078000697 | K926055 | 000 |
| 00709078000706 | K926055 | 000 |
| 10709078000819 | K926055 | 000 |
| 00709078000843 | K926055 | 000 |
| 00709078000775 | K926055 | 000 |