FDA 510(k)

INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER

K-Number: K983604 · 1999-05-27

Decision Date1999-05-27

Product CodeMQF

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER is the device name listed in this FDA 510(k) record. The listed applicant is Washington Regulatory Services. It received FDA 510(k) clearance on 1999-05-27 under 510(k) number K983604. The device is classified under product code MQF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER?

INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER is a medical device that received FDA 510(k) clearance on 1999-05-27. The listed applicant is Washington Regulatory Services. The 510(k) number is K983604.

When did INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER receive FDA 510(k) clearance?

INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER received FDA 510(k) clearance on 1999-05-27, under 510(k) number K983604.

Who is the listed applicant for INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER?

The FDA 510(k) record lists Washington Regulatory Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER?

The FDA product code for INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER is MQF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.