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Stebar Instrument Corp.

FDA Regulatory Profile

Stebar Instrument Corp. 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 June 12, 1995.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K952266SCHROEDER ORAL/NASAL DIRECTIONAL STYLETTEJune 12, 1995
K935797SCHROEDER ORAL/NASAL DIRECTIONAL STYLETTEJanuary 12, 1994

FDA data resources