Precision Dynamics Corporation

Precision Dynamics Corporation holds 1 FDA 510(k) medical device clearance, cleared in 2016, with 1 FDA device recall on record.

FDA recalls by Precision Dynamics Corporation

Z-1872-2013 — Non-sterile Viscot Surgical Skin Markers Part Number 1437-100 Non-sterile Viscot Part Number 143-100 Surgical Skin Markers are pen-like devices intended to be used to write on the patient's skin, e.g., to outline surgical incision sites or mark anatomical sites for accurate blood pressure measurement; available in nonsterile configuration.Class II·Terminated·2013-07-10

Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.

Recent clearances by Precision Dynamics Corporation

K161920 — Comfort CoverCode IZH·2016-07-15

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

Top product codes for Precision Dynamics Corporation

FDA recalls by Precision Dynamics Corporation

Recent clearances by Precision Dynamics Corporation