• 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 Laparoscope, General & Plastic Surgery
510(k) Number K161720
Device Name Standard Clamp
Applicant
STANDARD BARIATRICS
4362 GLENDALE MILFORD RD.
CINCINNATI,  OH  45242
Applicant Contact Alison Sathe
Correspondent
STANDARD BARIATRICS
4362 GLENDALE MILFORD RD.
CINCINNATI,  OH  45242
Correspondent Contact Alison Sathe
Regulation Number876.1500
Classification Product Code
GCJ  
Date Received06/22/2016
Decision Date 10/24/2016
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-