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Arzbaecher & Co.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K800201
ESOPHAGEAL PILL-ELECTRODE
February 26, 1980
K792283
ESOPHAGEAL ECG PREAMPLIFIER & SIGNAL CON
November 21, 1979