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Oculinum, Inc.

FDA Regulatory Profile

Oculinum, 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 February 9, 1990.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K900098MONOPOLAR NEEDLE ELECTRODEFebruary 9, 1990
K900279OCULINUM INJECTION AMPLIFIERFebruary 9, 1990
K854793MONOPOLAR INJECTION NEEDLE ELECTRODEFebruary 18, 1986

FDA data resources