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Edgewater Medical Equipment Systems

FDA Regulatory Profile

Edgewater Medical Equipment Systems 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 11, 1987.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K873370ALLEN MALLEABLE ANESTHESIA SCREENSeptember 11, 1987
K872900THE PORTABLE ORDERLYAugust 21, 1987
K860177ALLEN UNIVERSAL STIRRUPFebruary 11, 1986

FDA data resources