FDA 510(k) Applications Submitted by SHANGHAI COSMOS CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K992271 07/07/1999 PRE-POWDERED VINYL PATIENT EXAMINATION GLOVES SHANGHAI COSMOS CORP.
K992272 07/07/1999 POWDER-FREE VINYL PATIENT EXAMINATION GLOVES SHANGHAI COSMOS CORP.


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