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 forceps, biopsy, electric
510(k) Number K905088
Device Name HOT BIOPSY FORCEPS
Applicant
ESCO PRECISION, INC.
21 WILLIAM PENN DR.
STONY BROOK,  NY  11790
Applicant Contact TED ESSER
Correspondent
ESCO PRECISION, INC.
21 WILLIAM PENN DR.
STONY BROOK,  NY  11790
Correspondent Contact TED ESSER
Regulation Number876.4300
Classification Product Code
KGE  
Date Received11/14/1990
Decision Date 03/19/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-