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FDA 510(k) Applications Submitted by MEMTEC CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K102723
09/21/2010
MODEL 950-12L HOLTER RECORDER WITHOUT ANALYSIS
MEMTEC CORP.
K103427
11/22/2010
MOBILEECG SYSTEM
MEMTEC CORP.
K944180
08/26/1994
MODEL 700
MEMTEC CORP.
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