Beecher Medical Diagnostic Instrumentation

FDA Regulatory Profile

Beecher Medical Diagnostic Instrumentation 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 September 9, 1987.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K871830NAPSAC(TM)September 9, 1987
K850288HEPATIC PARENCHYMAL SUCTION DISSECTORMarch 18, 1985
K833800BEECHER 20 GA. PROBEJanuary 4, 1984