TUCKER EMBRYO CATHETER
K-Number: K023017 · 2002-12-13
Advertisement
Device Summary
Frequently Asked Questions
What is the TUCKER EMBRYO CATHETER?
TUCKER EMBRYO CATHETER is a medical device that received FDA 510(k) clearance on 2002-12-13. The listed applicant is Fertility Technology Resources, Inc.. The 510(k) number is K023017.
When did TUCKER EMBRYO CATHETER receive FDA 510(k) clearance?
TUCKER EMBRYO CATHETER received FDA 510(k) clearance on 2002-12-13, under 510(k) number K023017.
Who is the listed applicant for TUCKER EMBRYO CATHETER?
The FDA 510(k) record lists Fertility Technology Resources, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUCKER EMBRYO CATHETER?
The FDA product code for TUCKER EMBRYO CATHETER is MQF.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Fertility Technology Resources, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MQF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.
Advertisement