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Proto-Med, Inc.

FDA Regulatory Profile

Proto-Med, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 27, 1984.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K844852THE GENERIC OXYGEN CONCENTRATORDecember 27, 1984
K822301ROYAL 1 OXYGEN CONCENTRATORAugust 19, 1982
K820115EMMETT IUD THREAD RETREIVERFebruary 5, 1982
K811761THE EMMETT IUD THREAD RETRIEVERSeptember 21, 1981

FDA data resources