Needle, Assisted Reproduction

What Is FDA Product Code MQE?

Needle, Assisted Reproduction is FDA product code MQE, Class 2, 21 CFR 884.6100.

What Does It Take to Sell It in the United States?

A 510(k) premarket notification is required before it is sold in the United States: the applicant shows the device is substantially equivalent to one already on the market. The review can be done by an FDA-accredited third party, which is usually faster. Chinese applicants hold 3 clearances under this code; the FDA took a median of 263 days from receipt to decision on them.

What Do the Recalls Say?

The FDA has recorded 1 recall under this product code since 2008. None was by a company in China. The root cause the FDA records most often is Packaging (1).

A recall is a fact about one product and its maker, not a grade for every manufacturer of the type.