AARON ARTHROSCOPY ELECTRODE, CATALOG NUMBERS AR00, AR01, AR02, AND AR03

Electrosurgical, Cutting & Coagulation & Accessories

AARON MEDICAL INDUSTRIES

The following data is part of a premarket notification filed by Aaron Medical Industries with the FDA for Aaron Arthroscopy Electrode, Catalog Numbers Ar00, Ar01, Ar02, And Ar03.

Pre-market Notification Details

Device IDK020579
510k NumberK020579
Device Name:AARON ARTHROSCOPY ELECTRODE, CATALOG NUMBERS AR00, AR01, AR02, AND AR03
ClassificationElectrosurgical, Cutting & Coagulation & Accessories
Applicant AARON MEDICAL INDUSTRIES 7100 30TH AVE. NORTH St. Petersburg,  FL  33710 -2902
ContactRichard A Kozloff
CorrespondentRichard A Kozloff
AARON MEDICAL INDUSTRIES 7100 30TH AVE. NORTH St. Petersburg,  FL  33710 -2902
Product CodeGEI  
CFR Regulation Number878.4400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2002-02-21
Decision Date2002-05-13
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
50749756277339 K020579 000
00887482177631 K020579 000
00887482177655 K020579 000
00887482181492 K020579 000
20884524000128 K020579 000
20884524000135 K020579 000
20884524000142 K020579 000
20884524000470 K020579 000
20884524000487 K020579 000
20884524000036 K020579 000
50749756267392 K020579 000
50749756277278 K020579 000
50749756277322 K020579 000
00887482177617 K020579 000

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