• 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 Dressing, Wound, Drug
510(k) Number K203835
FOIA Releasable 510(k) K203835
Device Name MIS Solution
Applicant
Next Science, LLC
10550 Deerwood Park Blvd., Suite 300
Jacksonsonville,  FL  32256
Applicant Contact Courtney Narain
Correspondent
Next Science, LLC
10550 Deerwood Park Blvd., Suite 300
Jacksonsonville,  FL  32256
Correspondent Contact Courtney Narain
Classification Product Code
FRO  
Date Received12/30/2020
Decision Date 04/23/2021
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product Yes
Predetermined Change
Control Plan Authorized
No
-
-