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Endotronics, Inc.

FDA Regulatory Profile

Endotronics, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 12, 1988.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K875151ACUSYST-P/3XJanuary 12, 1988
K872086ACUSYST-JRJune 15, 1987
K864334ACUSYST-P (CELL CULTURE EQUIPMENT)November 24, 1986

FDA data resources