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Parker Quality & Compliance

PQC Reg Watch

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Device type

Eye Tray

Product code OJK · Class II · 21 CFR 886.4790 · Ophthalmic

This product code has been established in accordance with the May 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

FDA classification database

Recent 510(k)s

No 510(k) clearances in the archive for OJK.

Recent recalls