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FDA 510(k)

OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138

K-Number: K992308 · 1999-09-13

ApplicantLifetek Medical, Inc.
Decision Date1999-09-13
Product CodeMQE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138 is the device name listed in this FDA 510(k) record. The listed applicant is Lifetek Medical, Inc.. It received FDA 510(k) clearance on 1999-09-13 under 510(k) number K992308. 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 RETRIEVAL NEEDLE SET, MODEL 90138?

OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138 is a medical device that received FDA 510(k) clearance on 1999-09-13. The listed applicant is Lifetek Medical, Inc.. The 510(k) number is K992308.

When did OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138 receive FDA 510(k) clearance?

OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138 received FDA 510(k) clearance on 1999-09-13, under 510(k) number K992308.

Who is the listed applicant for OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138?

The FDA 510(k) record lists Lifetek Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138?

The FDA product code for OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138 is MQE.

Related Clinical Trials

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Other records listing Lifetek Medical, 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.

K921518LIFETEK IUI CATHETER

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

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