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 Airway, Oropharyngeal, Anesthesiology
510(k) Number K881065
Device Name RESUS-AID
Applicant
Applied Convergent Technologies, Inc.
15139 Don Julian Rd.
City Of Industry,  CA  91747
Applicant Contact WING G LEW
Correspondent
Applied Convergent Technologies, Inc.
15139 Don Julian Rd.
City Of Industry,  CA  91747
Correspondent Contact WING G LEW
Regulation Number868.5110
Classification Product Code
CAE  
Date Received03/14/1988
Decision Date 07/14/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-