COOPERSURGICAL OOCYTE RECOVERY NEEDLES
K-Number: K023930 · 2003-01-22
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Device Summary
Frequently Asked Questions
What is the COOPERSURGICAL OOCYTE RECOVERY NEEDLES?
COOPERSURGICAL OOCYTE RECOVERY NEEDLES is a medical device that received FDA 510(k) clearance on 2003-01-22. The listed applicant is CooperSurgical, Inc.. The 510(k) number is K023930.
When did COOPERSURGICAL OOCYTE RECOVERY NEEDLES receive FDA 510(k) clearance?
COOPERSURGICAL OOCYTE RECOVERY NEEDLES received FDA 510(k) clearance on 2003-01-22, under 510(k) number K023930.
Who is the listed applicant for COOPERSURGICAL OOCYTE RECOVERY NEEDLES?
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 COOPERSURGICAL OOCYTE RECOVERY NEEDLES?
The FDA product code for COOPERSURGICAL OOCYTE RECOVERY NEEDLES is MQE.
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 CooperSurgical, 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: MQE)
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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