REPROCESSED COMPRESSION SLEEVES

Sleeve, Limb, Compressible

ALLIANCE MEDICAL CORP.

The following data is part of a premarket notification filed by Alliance Medical Corp. with the FDA for Reprocessed Compression Sleeves.

Pre-market Notification Details

Device IDK024074
510k NumberK024074
Device Name:REPROCESSED COMPRESSION SLEEVES
ClassificationSleeve, Limb, Compressible
Applicant ALLIANCE MEDICAL CORP. 10232 SOUTH 51ST ST. Phoenix,  AZ  85044
ContactMoira Barton
CorrespondentMoira Barton
ALLIANCE MEDICAL CORP. 10232 SOUTH 51ST ST. Phoenix,  AZ  85044
Product CodeJOW  
CFR Regulation Number870.5800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2002-12-10
Decision Date2003-03-07
Summary:summary

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