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Mitsubishi Cable America, Inc.

FDA Regulatory Profile

Mitsubishi Cable America, 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 April 18, 1996.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K955717ENDOSCOPE INTRODUCER KITApril 18, 1996
K960081BATTERY POWERED ENDOSCCOPIC LIGHT SOURCEMarch 12, 1996
K936257ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3March 24, 1994

FDA data resources