• 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 collector, ostomy
510(k) Number K870531
Device Name EZ TAC FILTER
Applicant
JOHN F. GREER CO., INC.
530 E. 12TH ST.
OAKLAND,  CA  94606
Applicant Contact L. H GREER
Correspondent
JOHN F. GREER CO., INC.
530 E. 12TH ST.
OAKLAND,  CA  94606
Correspondent Contact L. H GREER
Regulation Number876.5900
Classification Product Code
EXB  
Date Received02/06/1987
Decision Date 04/10/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-