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 bandage, liquid
510(k) Number K990906
Device Name FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER
Applicant
FERRIS MFG. CORP.
16 WEST 300 83RD ST.
BURR RIDGE,  IL  60527
Applicant Contact THEODORE R THORSON
Correspondent
FERRIS MFG. CORP.
16 WEST 300 83RD ST.
BURR RIDGE,  IL  60527
Correspondent Contact THEODORE R THORSON
Regulation Number880.5090
Classification Product Code
KMF  
Date Received03/18/1999
Decision Date 04/29/1999
Decision SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-