WM Gloves get the 510(k) certification from FDA

We are proud to announce we just got the FDA 510(k) certification.

“We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA).”

It is a great step for WM Gloves that leads us to continue improving the quality of all our products.

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