The following data is part of a premarket notification filed by Innovative Medical Systems, Inc. with the FDA for Bazooka System.
| Device ID | K951469 |
| 510k Number | K951469 |
| Device Name: | BAZOOKA SYSTEM |
| Classification | Mattress, Air Flotation, Alternating Pressure |
| Applicant | INNOVATIVE MEDICAL SYSTEMS, INC. 1050 PERIMETER RD. Manchester, NH 03103 |
| Contact | Tom Asacker |
| Correspondent | Tom Asacker INNOVATIVE MEDICAL SYSTEMS, INC. 1050 PERIMETER RD. Manchester, NH 03103 |
| Product Code | FNM |
| CFR Regulation Number | 880.5550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-03-30 |
| Decision Date | 1995-06-28 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BAZOOKA SYSTEM 74471852 1887049 Dead/Cancelled |
Innovative Medical Systems, Inc. 1993-12-17 |