COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER
K-Number: K023383 · 2002-12-13
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Device Summary
Frequently Asked Questions
What is the COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER?
COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER is a medical device that received FDA 510(k) clearance on 2002-12-13. The listed applicant is Cooper Surgical. The 510(k) number is K023383.
When did COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER receive FDA 510(k) clearance?
COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER received FDA 510(k) clearance on 2002-12-13, under 510(k) number K023383.
Who is the listed applicant for COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER?
The FDA 510(k) record lists Cooper Surgical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER?
The FDA product code for COOPERSURGICAL INTRAUTERINE INSEMINATION 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 Cooper Surgical 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.
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