FDA 510(k) Applications Submitted by JOHN C HEINMILLER

FDA 510(k) Number Submission Date Device Name Applicant
K962805 07/18/1996 SPYGLASS ANGIOGRAPHIC CATHETER DAIG CORP.
K964518 10/25/1996 FAST-CATH TRANSSEPTAL CATHETER INTRODUCER DAIG CORP.
K965249 12/12/1996 SPYGLASS ANGIOGRAPHIC CATHETER DAIG CORP.


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