NUMOBAG
Chamber, Oxygen, Topical, Extremity
NUMOTECH, INC.
The following data is part of a premarket notification filed by Numotech, Inc. with the FDA for Numobag.
Pre-market Notification Details
| Device ID | K981949 |
| 510k Number | K981949 |
| Device Name: | NUMOBAG |
| Classification | Chamber, Oxygen, Topical, Extremity |
| Applicant | NUMOTECH, INC. 21800 OXNARD ST., SUITE 840 WARNER CENTER PLAZA Woodland Hills, CA 91367 |
| Contact | W. Patrick Noonan |
| Correspondent | W. Patrick Noonan NUMOTECH, INC. 21800 OXNARD ST., SUITE 840 WARNER CENTER PLAZA Woodland Hills, CA 91367 |
| Product Code | KPJ |
| CFR Regulation Number | 878.5650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-06-03 |
| Decision Date | 1999-02-03 |
Trademark Results [NUMOBAG]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NUMOBAG 85585375 4490163 Live/Registered |
Numotech, Inc. 2012-03-30 |
 NUMOBAG 76035643 2463757 Dead/Cancelled |
NUMOTECH, INC. 2000-04-27 |
 NUMOBAG 75285899 not registered Dead/Abandoned |
Numotech, Inc. 1997-05-05 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.