• 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 Disinfectant, Medical Devices
510(k) Number K953241
Device Name EXSPOR
Applicant
Alcide Corp.
8561 154th Ave., NE
Redmond,  WA  98052
Applicant Contact JOHN P RICHARDS
Correspondent
Alcide Corp.
8561 154th Ave., NE
Redmond,  WA  98052
Correspondent Contact JOHN P RICHARDS
Regulation Number880.6890
Classification Product Code
LRJ  
Date Received07/11/1995
Decision Date 09/29/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel Gastroenterology/Urology
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-