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 hysteroscope (and accessories)
510(k) Number K881249
Device Name BAGGISH, HYSTEROSCOPE
Applicant
BRYAN CORP.
FOUR PLYMPTON ST.
WOBURN,  MA  01801
Applicant Contact FRANK M ABRANO
Correspondent
BRYAN CORP.
FOUR PLYMPTON ST.
WOBURN,  MA  01801
Correspondent Contact FRANK M ABRANO
Regulation Number884.1690
Classification Product Code
HIH  
Date Received03/23/1988
Decision Date 07/28/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-