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FDA 510(k) Applications Submitted by DOUGLAS MEDICAL PRODUCTS CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K961155
03/22/1996
SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908
DOUGLAS MEDICAL PRODUCTS CORP.
K954428
09/22/1995
SOLOPICC 24 (60CM) 20GA CATHETER
DOUGLAS MEDICAL PRODUCTS CORP.
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