510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K840725Substantially Equivalent

Clinical Care Stimulator

Biostim, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K840725 is the FDA 510(k) clearance record for CLINICAL CARE STIMULATOR, cleared for Biostim, Inc. on . FDA records list 5 510(k) clearances for Biostim, Inc., from to . As of , FDA records show no recalls naming K840725.

Clearance record

Decision date
Received
(57 days to decision)
Review panel
Unknown
Applicant
Biostim, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No