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FDA 510(k)

OOCYTE ASPIRATION NEEDLE

K-Number: K991271 · 2000-03-08

ApplicantCasmed UK
Decision Date2000-03-08
Product CodeMQE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OOCYTE ASPIRATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Casmed UK. It received FDA 510(k) clearance on 2000-03-08 under 510(k) number K991271. The device is classified under product code MQE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OOCYTE ASPIRATION NEEDLE?

OOCYTE ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 2000-03-08. The listed applicant is Casmed UK. The 510(k) number is K991271.

When did OOCYTE ASPIRATION NEEDLE receive FDA 510(k) clearance?

OOCYTE ASPIRATION NEEDLE received FDA 510(k) clearance on 2000-03-08, under 510(k) number K991271.

Who is the listed applicant for OOCYTE ASPIRATION NEEDLE?

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

What is the FDA product code for OOCYTE ASPIRATION NEEDLE?

The FDA product code for OOCYTE ASPIRATION NEEDLE is MQE.

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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.

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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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