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FDA 510(k) Applications Submitted by DIEMOLDING CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K961455
04/16/1996
MEDSHIELD/AEROCHAMBER
DIEMOLDING CORP.
K962749
07/15/1996
THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK, RESISTOR/PORT/MOUTHPIECE, RESISTOR/PORT
DIEMOLDING CORP.
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