FDA 510(k)

INTRATUBAL TRANSFER SETS

K-Number: K983591 · 1998-12-21

Decision Date1998-12-21

Product CodeMQF

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

INTRATUBAL TRANSFER 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 K983591. 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 INTRATUBAL TRANSFER SETS?

INTRATUBAL TRANSFER 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 K983591.

When did INTRATUBAL TRANSFER SETS receive FDA 510(k) clearance?

INTRATUBAL TRANSFER SETS received FDA 510(k) clearance on 1998-12-21, under 510(k) number K983591.

Who is the listed applicant for INTRATUBAL TRANSFER 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 INTRATUBAL TRANSFER SETS?

The FDA product code for INTRATUBAL TRANSFER 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.