• 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 arthroscope
510(k) Number K820777
Device Name MINI-MICRO ARTHROSCOPIC SCAPEL
Applicant
THE ANSPACH EFFORT, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
THE ANSPACH EFFORT, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number888.1100
Classification Product Code
HRX  
Date Received03/23/1982
Decision Date 05/12/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-