• 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 Tray, Surgical, Instrument
510(k) Number K905682
Device Name RICHARD-ALLAN CLAMP COVERS
Applicant
RICHARD-ALLAN MEDICAL
8850M89, BOX 351
RICHLAND,  MI  49083
Applicant Contact DAVE COLE
Correspondent
RICHARD-ALLAN MEDICAL
8850M89, BOX 351
RICHLAND,  MI  49083
Correspondent Contact DAVE COLE
Regulation Number878.4800
Classification Product Code
FSM  
Date Received12/19/1990
Decision Date 02/19/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-