GLASS VIALS
Container, I.v.
MEDI-PLAST INTL., INC.
The following data is part of a premarket notification filed by Medi-plast Intl., Inc. with the FDA for Glass Vials.
Pre-market Notification Details
| Device ID | K811269 |
| 510k Number | K811269 |
| Device Name: | GLASS VIALS |
| Classification | Container, I.v. |
| Applicant | MEDI-PLAST INTL., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPE |
| CFR Regulation Number | 880.5025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-05-05 |
| Decision Date | 1981-06-16 |
Trademark Results [GLASS VIALS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 GLASS VIALS 86966758 not registered Dead/Abandoned |
Scientific Specialties Service, Inc. 2016-04-06 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.