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Swemed Laboratories, Inc.

FDA Regulatory Profile

Swemed Laboratories, Inc. 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 August 19, 1986.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K862364NEEDLE GUIDE (FOR ULTRASOUND TRANSDUCERS)August 19, 1986
K862365NEEDLE FOR AMNIOCENTESIS AND CYST PUNCTUREJuly 7, 1986

FDA data resources