BAG DECANTER
Container, I.v.
SUPERIOR MEDICAL PRODUCTS
The following data is part of a premarket notification filed by Superior Medical Products with the FDA for Bag Decanter.
Pre-market Notification Details
| Device ID | K890272 |
| 510k Number | K890272 |
| Device Name: | BAG DECANTER |
| Classification | Container, I.v. |
| Applicant | SUPERIOR MEDICAL PRODUCTS P.O. BOX 99 Mccaysville, GA 30555 |
| Contact | Cottone, Jr |
| Correspondent | Cottone, Jr SUPERIOR MEDICAL PRODUCTS P.O. BOX 99 Mccaysville, GA 30555 |
| Product Code | KPE |
| CFR Regulation Number | 880.5025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-18 |
| Decision Date | 1989-03-14 |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20680211002570 | K890272 | 000 |
| 00680211000473 | K890272 | 000 |
| 00680211000015 | K890272 | 000 |
Trademark Results [BAG DECANTER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BAG DECANTER 73610527 not registered Dead/Abandoned |
MEDI-PLAST INTERNATIONAL, INC. 1986-07-21 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.