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 Basin, Emesis
510(k) Number K792625
Device Name STERILIZATION PROCESS/PLACENTA BASIN
Applicant
Procter & Gamble Mfg. Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Procter & Gamble Mfg. Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.6730
Classification Product Code
FNY  
Date Received12/19/1979
Decision Date 01/16/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-