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FDA 510(k)

EMBRYO FREEZE MEDIUM, EMBRYO THAW MEDIUM

K-Number: K013518 · 2002-01-18

ApplicantIrvine Scientific Sales Co., Inc.
Decision Date2002-01-18
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

EMBRYO FREEZE MEDIUM, EMBRYO THAW MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Irvine Scientific Sales Co., Inc.. It received FDA 510(k) clearance on 2002-01-18 under 510(k) number K013518. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMBRYO FREEZE MEDIUM, EMBRYO THAW MEDIUM?

EMBRYO FREEZE MEDIUM, EMBRYO THAW MEDIUM is a medical device that received FDA 510(k) clearance on 2002-01-18. The listed applicant is Irvine Scientific Sales Co., Inc.. The 510(k) number is K013518.

When did EMBRYO FREEZE MEDIUM, EMBRYO THAW MEDIUM receive FDA 510(k) clearance?

EMBRYO FREEZE MEDIUM, EMBRYO THAW MEDIUM received FDA 510(k) clearance on 2002-01-18, under 510(k) number K013518.

Who is the listed applicant for EMBRYO FREEZE MEDIUM, EMBRYO THAW MEDIUM?

The FDA 510(k) record lists Irvine Scientific Sales Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMBRYO FREEZE MEDIUM, EMBRYO THAW MEDIUM?

The FDA product code for EMBRYO FREEZE MEDIUM, EMBRYO THAW MEDIUM is MQL.

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Related Devices (Code: MQL)

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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