INSTAFIL
Container, I.v.
INSTAFIL, INC.
The following data is part of a premarket notification filed by Instafil, Inc. with the FDA for Instafil.
Pre-market Notification Details
| Device ID | K810795 |
| 510k Number | K810795 |
| Device Name: | INSTAFIL |
| Classification | Container, I.v. |
| Applicant | INSTAFIL, 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 | 1981-03-23 |
| Decision Date | 1981-06-12 |
Trademark Results [INSTAFIL]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INSTAFIL 78622543 not registered Dead/Abandoned |
Henkel Consumer Adhesives, Inc. 2005-05-04 |
 INSTAFIL 73301313 1203429 Dead/Expired |
Instafil, Inc. 1981-03-16 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.