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FDA 510(k)

WALLACE ARTIFICIAL INSEMINATION CATHETER

K-Number: K061679 · 2006-10-13

ApplicantIrvine Scientific Sales Co., Inc.
Decision Date2006-10-13
Product CodeLKF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WALLACE ARTIFICIAL INSEMINATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Irvine Scientific Sales Co., Inc.. It received FDA 510(k) clearance on 2006-10-13 under 510(k) number K061679. The device is classified under product code LKF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALLACE ARTIFICIAL INSEMINATION CATHETER?

WALLACE ARTIFICIAL INSEMINATION CATHETER is a medical device that received FDA 510(k) clearance on 2006-10-13. The listed applicant is Irvine Scientific Sales Co., Inc.. The 510(k) number is K061679.

When did WALLACE ARTIFICIAL INSEMINATION CATHETER receive FDA 510(k) clearance?

WALLACE ARTIFICIAL INSEMINATION CATHETER received FDA 510(k) clearance on 2006-10-13, under 510(k) number K061679.

Who is the listed applicant for WALLACE ARTIFICIAL INSEMINATION CATHETER?

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

What is the FDA product code for WALLACE ARTIFICIAL INSEMINATION CATHETER?

The FDA product code for WALLACE ARTIFICIAL INSEMINATION CATHETER is LKF.

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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.

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