Product code OKZ

Device name
Endometrial Sampling Kit
Medical specialty
Obstetrics/Gynecology
Device class
2
Regulation number
884.1175
Review panel
OB
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
N
Summary malfunction reporting
Eligible
Definition
This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. 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.
Source
FDA openFDA device classification dataset