510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K827069Substantially Equivalent

Podioscope by Arrow

Arrow X-Ray Corp., Seattle WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K827069 is the FDA 510(k) clearance record for PODIOSCOPE BY ARROW, cleared for Arrow X-Ray Corp. on . FDA records list 2 510(k) clearances for Arrow X-Ray Corp. As of , FDA records show no recalls naming K827069.

Clearance record

Decision date
Received
(31 days to decision)
Review panel
Unknown
Applicant
Arrow X-Ray Corp. 7129 39th Ave. SW, Seattle WA
Third party review
No