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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