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 K946082
Device Name BEECH PRO LOK FIXED
Applicant
Beech Medical Products, Inc.
241 Lackland Dr.
Middlesex,  NJ  08846
Applicant Contact JOHN ROMANO
Correspondent
Beech Medical Products, Inc.
241 Lackland Dr.
Middlesex,  NJ  08846
Correspondent Contact JOHN ROMANO
Regulation Number880.5440
Classification Product Code
FPA  
Date Received12/13/1994
Decision Date 03/13/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-