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
510(k) Number K861923
Device Name STERILE DISPOSABLE SUCTION TUBE CATHETER
Applicant
Pilling Co.
420 Delaware Dr.
Fort Washington,  PA  19034
Applicant Contact LELAND J WIMER
Correspondent
Pilling Co.
420 Delaware Dr.
Fort Washington,  PA  19034
Correspondent Contact LELAND J WIMER
Date Received05/19/1986
Decision Date 05/30/1986
Decision Substantially Equivalent (SESE)
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-