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 Camera, Television, Surgical, Without Audio
510(k) Number K902359
Device Name SURGICAL VIDEO CAMERA, MODEL 9500
Applicant
SEITZ TECHNICAL PRODUCTS, INC.
187 E. ASHLAND ST.
DOYLESTOWN,  PA  18901
Applicant Contact PATRICK MCVAY
Correspondent
SEITZ TECHNICAL PRODUCTS, INC.
187 E. ASHLAND ST.
DOYLESTOWN,  PA  18901
Correspondent Contact PATRICK MCVAY
Regulation Number878.4160
Classification Product Code
FWB  
Date Received05/29/1990
Decision Date 07/12/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-