510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K832371Substantially Equivalent

Egs Model 300

Electro-Med Health Industries, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832371 is the FDA 510(k) clearance record for EGS MODEL 300, cleared for Electro-Med Health Industries, Inc. on . FDA records list 6 510(k) clearances for Electro-Med Health Industries, Inc., from to . As of , FDA records show no recalls naming K832371.

Clearance record

Decision date
Received
(80 days to decision)
Review panel
Unknown
Applicant
Electro-Med Health Industries, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No