Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 set, administration, intravascular
510(k) Number K913076
Device Name I.V. INSTANT TIMER
Applicant
THE MASTER MEDICAL CORP.
C/O MCKENNA & CUNEO LAW OFFICE
1575 EYE STREET, N.W.
WASHINGTON,  DC  20005
Applicant Contact DONALD R STONE
Correspondent
THE MASTER MEDICAL CORP.
C/O MCKENNA & CUNEO LAW OFFICE
1575 EYE STREET, N.W.
WASHINGTON,  DC  20005
Correspondent Contact DONALD R STONE
Regulation Number880.5440
Classification Product Code
FPA  
Date Received07/11/1991
Decision Date 10/17/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-