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 Apparatus, Exhaust, Surgical
510(k) Number K930066
Device Name BUFFALO FILTER REPLACEMENT FILTER #BCCHAR
Applicant
Buffalo Filter Co., Inc.
8388 Bridlewood Dr.
E. Amherst,  NY  14051
Applicant Contact CLINTON R HOLLAND
Correspondent
Buffalo Filter Co., Inc.
8388 Bridlewood Dr.
E. Amherst,  NY  14051
Correspondent Contact CLINTON R HOLLAND
Regulation Number878.5070
Classification Product Code
FYD  
Date Received01/06/1993
Decision Date 11/12/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-