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Intertex Medical, Inc.

FDA Regulatory Profile

Intertex Medical, 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 July 20, 1995.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K952824NEO-LINK, DISPOSABLE NEONATAL AIR WAY CONNECTORJuly 20, 1995
K830711TRACHESTOMY & NASAL SUCTIONING KIT #-May 2, 1983

FDA data resources