• 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 Maggots, Medical
510(k) Number K033391
Device Name MEDICAL MAGGOTS
Applicant
RONALD A. SHERMAN
36 UREY COURT
IRVINE,  CA  92612
Applicant Contact RONALD A SHERMAN
Correspondent
RONALD A. SHERMAN
36 UREY COURT
IRVINE,  CA  92612
Correspondent Contact RONALD A SHERMAN
Classification Product Code
NQK  
Date Received10/23/2003
Decision Date 01/12/2004
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-