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 bedpan
510(k) Number K760307
Device Name BEDPAN, SINGLE PATIENT USE, TECNOL
Applicant
TECNOL NEW JERSEY WOUND CARE, INC.
368 FAIRVIEW AVE.
HAMMONTON,  NJ  08037 -0268
Correspondent
TECNOL NEW JERSEY WOUND CARE, INC.
368 FAIRVIEW AVE.
HAMMONTON,  NJ  08037 -0268
Regulation Number880.6730
Classification Product Code
FOB  
Date Received07/26/1976
Decision Date 08/11/1976
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-