The following data is part of a premarket notification filed by Ostex Intl., Inc. with the FDA for Osteomark.
Device ID | K961562 |
510k Number | K961562 |
Device Name: | OSTEOMARK |
Classification | Column Chromatography & Color Development, Hydroxyproline |
Applicant | OSTEX INTL., INC. 2203 AIRPORT WAY SOUTH SUITE 400 Seattle, WA 98134 |
Contact | Nancy Mallinak |
Correspondent | Nancy Mallinak OSTEX INTL., INC. 2203 AIRPORT WAY SOUTH SUITE 400 Seattle, WA 98134 |
Product Code | JMM |
CFR Regulation Number | 862.1400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-04-22 |
Decision Date | 1996-07-11 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OSTEOMARK 74801494 1819369 Live/Registered |
ALERE NORTH AMERICA, LLC 1990-09-24 |
OSTEOMARK 74099485 1819553 Live/Registered |
ALERE NORTH AMERICA, LLC 1990-09-24 |