510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K827704Substantially Equivalent

Mm-22 Microtron

Instrument AB Scanditronix, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K827704 is the FDA 510(k) clearance record for MM-22 MICROTRON, cleared for Instrument AB Scanditronix on . FDA records list one 510(k) clearance for Instrument AB Scanditronix. As of , FDA records show no recalls naming K827704.

Clearance record

Decision date
Received
(90 days to decision)
Review panel
Unknown
Applicant
Instrument AB Scanditronix 4221 Richmond Rd., NW, Walker MI
Third party review
No