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/ Protomed Corp.
Protomed Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Known Names
proto-med, protomed
Recent 510(k) Clearances
K-Number
Device
Date
K193499
DigiGuide System
November 4, 2020
K841986
PROTOMED/TOWIC NASOGASTRIC TUBE DRAINAGE BAG
September 10, 1984