FDA 510(k) Applications Submitted by ARISTA MEDI PRIMA

FDA 510(k) Number Submission Date Device Name Applicant
K963742 09/17/1996 LATEX EXAMINATION GLOVES, POWDERED ARISTA MEDI PRIMA
K970977 03/14/1997 LATEX EXAMINATION GLOVES, POWDER FREE ARISTA MEDI PRIMA
K964629 11/19/1996 VINYL PATIENT EXAMINATION GLOVES ARISTA MEDI PRIMA


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact