• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Column Chromatography & Color Development, Hydroxyproline
510(k) Number K961562
Device Name OSTEOMARK
Applicant
Ostex Intl., Inc.
2203 Airport Way S.
Suite 400
Seattle,  WA  98134
Applicant Contact NANCY MALLINAK
Correspondent
Ostex Intl., Inc.
2203 Airport Way S.
Suite 400
Seattle,  WA  98134
Correspondent Contact NANCY MALLINAK
Regulation Number862.1400
Classification Product Code
JMM  
Date Received04/22/1996
Decision Date 07/11/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-