The following data is part of a premarket notification filed by Instafil, Inc. with the FDA for Instafil.
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 |
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 |