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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K827571Substantially Equivalent

Mobile Digital Receptor

Technicare Corp., Solon OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K827571 is the FDA 510(k) clearance record for MOBILE DIGITAL RECEPTOR, cleared for Technicare Corp. on . FDA records list 32 510(k) clearances for Technicare Corp., from to . As of , FDA records show no recalls naming K827571.

Clearance record

Decision date
Received
(37 days to decision)
Review panel
Unknown
Applicant
Technicare Corp. 29100 Aurora Rd., Solon OH
Third party review
No