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Loseff Medical Designers, Ltd.

FDA Regulatory Profile

Loseff Medical Designers, Ltd. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 26, 1980.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K802025BALLOON RETENTION CHEST CATHETERSeptember 26, 1980
K801349LOSEFF BALLOON TYPE SELF-RETENTION WOUNDAugust 7, 1980

FDA data resources