• 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 retractor
510(k) Number K915175
Device Name REDDICK RETRACTOR
Applicant
IDEAL MEDICAL, INC.
12167 49TH ST. NORTH
P.O. BOX 17327
CLEARWATER,  FL  34622
Applicant Contact LORNA LINVILLE
Correspondent
IDEAL MEDICAL, INC.
12167 49TH ST. NORTH
P.O. BOX 17327
CLEARWATER,  FL  34622
Correspondent Contact LORNA LINVILLE
Regulation Number878.4800
Classification Product Code
GAD  
Date Received11/15/1991
Decision Date 04/29/1992
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
-
-