FDA 510(k)

WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N

K-Number: K990348 · 1999-07-26

Decision Date1999-07-26

Product CodeMQF

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N is the device name listed in this FDA 510(k) record. The listed applicant is CooperSurgical, Inc.. It received FDA 510(k) clearance on 1999-07-26 under 510(k) number K990348. 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 WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N?

WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N is a medical device that received FDA 510(k) clearance on 1999-07-26. The listed applicant is CooperSurgical, Inc.. The 510(k) number is K990348.

When did WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N receive FDA 510(k) clearance?

WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N received FDA 510(k) clearance on 1999-07-26, under 510(k) number K990348.

Who is the listed applicant for WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N?

The FDA 510(k) record lists CooperSurgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N?

The FDA product code for WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N 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.