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 |