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 Pump, Portable, Aspiration (Manual Or Powered)
510(k) Number K870094
Device Name BUNN MODEL 530 ASPIRATOR
Applicant
THE JOHN BUNN CO.
290 CREEKSIDE DR.
TONAWANDA,  NY  14150
Applicant Contact DENNIS KENYON
Correspondent
THE JOHN BUNN CO.
290 CREEKSIDE DR.
TONAWANDA,  NY  14150
Correspondent Contact DENNIS KENYON
Regulation Number878.4780
Classification Product Code
BTA  
Date Received01/09/1987
Decision Date 03/06/1987
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
-
-