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
SUBSCRIBE / SIGN IN
K790803Substantially Equivalent

Syringe Tonometer

Medicor USA, Ltd., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K790803 is the FDA 510(k) clearance record for SYRINGE TONOMETER, cleared for Medicor USA , Ltd. on . FDA records list 14 510(k) clearances for Medicor USA , Ltd., from to . As of , FDA records show no recalls naming K790803.

Clearance record

Decision date
Received
(64 days to decision)
Review panel
Unknown
Applicant
Medicor USA , Ltd. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No