ARGYLE AUTOTRANSFUSION BAG

Apparatus, Autotransfusion

SHERWOOD MEDICAL CO.

The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Argyle Autotransfusion Bag.

Pre-market Notification Details

Device IDK882757
510k NumberK882757
Device Name:ARGYLE AUTOTRANSFUSION BAG
ClassificationApparatus, Autotransfusion
Applicant SHERWOOD MEDICAL CO. 1915 OLIVE ST. St. Louis,  MO  63103 -1625
ContactCynthia Pestka
CorrespondentCynthia Pestka
SHERWOOD MEDICAL CO. 1915 OLIVE ST. St. Louis,  MO  63103 -1625
Product CodeCAC  
CFR Regulation Number868.5830 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1988-07-05
Decision Date1988-09-01

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