The following data is part of a premarket notification filed by Marquest Medical Products, Inc. with the FDA for Autostik.
Device ID | K820875 |
510k Number | K820875 |
Device Name: | AUTOSTIK |
Classification | Arterial Blood Sampling Kit |
Applicant | MARQUEST MEDICAL PRODUCTS, INC. 112 Inverness Circle Suite A Englewood, CO 80112 |
Contact | Robert J Mckinnon |
Correspondent | Robertj J Mckinnon MARQUEST MEDICAL PRODUCTS, INC. 112 Inverness Circle Suite A Englewood, CO 80112 |
Product Code | CBT |
CFR Regulation Number | 868.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-03-29 |
Decision Date | 1982-05-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AUTOSTIK 74619044 not registered Dead/Abandoned |
Dealer Specialties, Inc. 1995-01-09 |
AUTOSTIK 73331654 1248860 Dead/Cancelled |
Marquest Medical Products, Inc. 1981-10-08 |