510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K863162Substantially Equivalent

Vacu-Guard

Arbor Technologies, Inc., Ann Arbor MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863162 is the FDA 510(k) clearance record for VACU-GUARD, cleared for Arbor Technologies, Inc. on . FDA records list 10 510(k) clearances for Arbor Technologies, Inc., from to . As of , FDA records show no recalls naming K863162.

Clearance record

Decision date
Received
(11 days to decision)
Review panel
Unknown
Applicant
Arbor Technologies, Inc. 3728-1 Plz. Dr., Ann Arbor MI
Third party review
No