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Pegasus Medical Supply, Inc.

FDA Regulatory Profile

Pegasus Medical Supply, Inc. has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
May 10, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K173012ANGIO-PRESS LITE DVT Compression DeviceMay 10, 2018
K143202ANGIO-PRESS DVT Compression Device Model Name: IPCSJul 7, 2015

FDA data resources