DeviceClearance

Product code OJA— General Hospital

MODEL CC-72 CAVERNOSOMETRY/CAVERNOSOGRAPHY SET

Classification name
Intravenous Extension Tubing Set
Device class
Class 2
Regulation
21 CFR 880.5440
Advisory panel
General Hospital
Total cleared
1
First cleared
Most recent

FDA classification 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.”

— U.S. Food and Drug Administration, device classification record for product code OJA under 21 CFR 880.5440, via openFDA

Market context for product code OJA

FDA has cleared 1 device under product code OJA, all in 1987, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Top applicants under product code OJA

Recent clearances under product code OJA

Data sourced from openFDA. This site is unofficial and independent of the FDA.