FDA 510(k)

EMBRYO TRANSFER CATHETERS/SETS

K-Number: K983594 · 1998-12-21

Decision Date1998-12-21

Product CodeMQF

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

EMBRYO TRANSFER CATHETERS/SETS is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ob/Gyn. It received FDA 510(k) clearance on 1998-12-21 under 510(k) number K983594. 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 EMBRYO TRANSFER CATHETERS/SETS?

EMBRYO TRANSFER CATHETERS/SETS is a medical device that received FDA 510(k) clearance on 1998-12-21. The listed applicant is Cook Ob/Gyn. The 510(k) number is K983594.

When did EMBRYO TRANSFER CATHETERS/SETS receive FDA 510(k) clearance?

EMBRYO TRANSFER CATHETERS/SETS received FDA 510(k) clearance on 1998-12-21, under 510(k) number K983594.

Who is the listed applicant for EMBRYO TRANSFER CATHETERS/SETS?

The FDA 510(k) record lists Cook Ob/Gyn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMBRYO TRANSFER CATHETERS/SETS?

The FDA product code for EMBRYO TRANSFER CATHETERS/SETS is MQF.

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Official Source

View on FDA Database →

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