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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K827525Substantially Equivalent

Automatic Exposure Control Type A3300

Advanced Instrument Development, Inc., Melrose Park IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K827525 is the FDA 510(k) clearance record for AUTOMATIC EXPOSURE CONTROL TYPE A3300, cleared for Advanced Instrument Development, Inc. on . FDA records list 5 510(k) clearances for Advanced Instrument Development, Inc., from to . As of , FDA records show no recalls naming K827525.

Clearance record

Decision date
Received
(28 days to decision)
Review panel
Unknown
Applicant
Advanced Instrument Development, Inc. 1011 N. 25th Ave., Melrose Park IL
Third party review
No