• 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 circuit, breathing (w connector, adaptor, y piece)
510(k) Number K871386
Device Name BREATHING CIRCUIT
Applicant
DRYDEN CORP.
10640 EAST 59TH ST.
P.O. BOX 36038
INDIANAPOLIS,  IN  46236
Applicant Contact PAUL E DRYDEN
Correspondent
DRYDEN CORP.
10640 EAST 59TH ST.
P.O. BOX 36038
INDIANAPOLIS,  IN  46236
Correspondent Contact PAUL E DRYDEN
Regulation Number868.5240
Classification Product Code
CAI  
Date Received04/07/1987
Decision Date 05/29/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-