• 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 Bedpan
510(k) Number K780370
Device Name STAND UP TOILET
Applicant
Medical Specialty Products, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Medical Specialty Products, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.6730
Classification Product Code
FOB  
Date Received03/07/1978
Decision Date 04/10/1978
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
-
-