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 Connector, Airway (Extension)
510(k) Number K860882
Device Name DISPOSABLE CATHETER
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
DIVISION OF DIEMOLDING CORP.
CANASTOTA,  NY  13032
Applicant Contact RONALD N MCHENRY
Correspondent
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
DIVISION OF DIEMOLDING CORP.
CANASTOTA,  NY  13032
Correspondent Contact RONALD N MCHENRY
Regulation Number868.5810
Classification Product Code
BZA  
Date Received02/25/1986
Decision Date 03/20/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-