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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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