510(k) K033391

Device
MEDICAL MAGGOTS
Applicant
RONALD A. SHERMAN
510(k) number
K033391
Product code
NQK  
Decision
Substantially Equivalent (SESE)
Decision date
2004-01-12
Date received
2003-10-23
Regulation
510(k) Premarket Notification
Classification name
Maggots, Medical
Medical specialty
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices
Review panel
General & Plastic Surgery
Device class
U
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
RONALD A SHERMAN
Address
36 Urey Ct. Irvine CA US 92612 92612

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code NQK  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K142020LARVAL DEBRIDEMENT THERAPY PRODUCTS - LARVAE 100/200/300 AND BIOBAG 50/100/200/300/400Biomonde2014-11-05
K131221LARVAL DEBRIDEMENT THERAPY PRODUCTS - BIOBAG 50/100/200/300/400Biomonde2013-08-28
K123449BIOMONDE LARVAEBiomonde (A Trading Name of Zoobiotic Limited)2013-03-05
K102827MEDICAL MAGGOTS, LESOCMonarch Labs, LLC2011-11-02
K072438MEDICAL MAGGOTS, CREATURE COMFORTSMonarch Labs, LLC2007-10-05

Legacy Summary#

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FDA Review#

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