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Keller Instruments, Inc.

FDA Regulatory Profile

Keller Instruments, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 17, 1985.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K854541TIP OFF FORCEPSDecember 17, 1985
K841294ACU220 CRYO UNITAugust 15, 1984
K841292SPECTACLE INDIRECT OPHTHALMOSCOPEMay 9, 1984
K841293PANORAMIC LOUPES - VARIOUSMay 9, 1984
K823835SPEMBLY 140 CRYOSYSTEM PROBES & TIPSJanuary 17, 1983

FDA data resources