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Howard Instruments, Inc.

FDA Regulatory Profile

Howard Instruments, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 4 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on May 16, 2007.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
4
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K063104FOX MEDICAL DIODE LASER SYSTEM 810NMMay 16, 2007
K030948VMATE MODEL VMM1000June 17, 2003
K980985SCMD-1000May 1, 1998
K974598MICROKERATOME OR THE MATEApril 22, 1998
K972727CBALK-1000 BLADEOctober 10, 1997

FDA data resources