• 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 Hysteroscope (And Accessories)
510(k) Number K102686
Device Name MYOSURE ROD LENS SCOPE SEALS
Applicant
INTERLACE MEDICAL, INC.
139 NEWBURY STREET
FRAMINGHAM,  MA  01701
Applicant Contact JOHN J VOZELLA
Correspondent
INTERLACE MEDICAL, INC.
139 NEWBURY STREET
FRAMINGHAM,  MA  01701
Correspondent Contact JOHN J VOZELLA
Regulation Number884.1690
Classification Product Code
HIH  
Date Received09/17/2010
Decision Date 10/15/2010
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
-
-