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Proto-Med, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K844852
THE GENERIC OXYGEN CONCENTRATOR
December 27, 1984
K822301
ROYAL 1 OXYGEN CONCENTRATOR
August 19, 1982
K820115
EMMETT IUD THREAD RETREIVER
February 5, 1982
K811761
THE EMMETT IUD THREAD RETRIEVER
September 21, 1981