MAXI-FLOW
Tube, Aspirating, Flexible, Connecting
BIO-MEDICAL DEVICES, INC.
The following data is part of a premarket notification filed by Bio-medical Devices, Inc. with the FDA for Maxi-flow.
Pre-market Notification Details
| Device ID | K955150 |
| 510k Number | K955150 |
| Device Name: | MAXI-FLOW |
| Classification | Tube, Aspirating, Flexible, Connecting |
| Applicant | BIO-MEDICAL DEVICES, INC. 1752-A LANGLEY AVE. Irvine, CA 92614 |
| Contact | Nick Herbert |
| Correspondent | Nick Herbert BIO-MEDICAL DEVICES, INC. 1752-A LANGLEY AVE. Irvine, CA 92614 |
| Product Code | BYY |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-11-13 |
| Decision Date | 1996-01-23 |
Trademark Results [MAXI-FLOW]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MAXI-FLOW 74011867 not registered Dead/Abandoned |
ANGIOMED AKTIENGELSELLSCHAFT 1989-12-18 |
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