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FDA 510(k) Applications Submitted by MEDI-TECH INTL. CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K002666
08/25/2000
DIAMOND ALOE VERA, STERILE
MEDI-TECH INTL. CORP.
K110377
02/09/2011
PROTECTIVE RESTRAINT
MEDI-TECH INTL. CORP.
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