Zdrowie i gospodarka · 10/09/1998

FDA Announces Draft Guidance for Devices Used in IVF and Assisted Reproduction Procedures

The FDA has released a draft guidance outlining the requirements for submitting a 510(k) premarket notification for medical devices used in in vitro fertilization (IVF) and related assisted reproduction procedures.

Source: Federal Register — Food and Drug AdministrationOpen original release →

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