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FDA 510(k)

EMBRYO BIOPSY MEDIUM

K-Number: K021358 · 2002-07-05

ApplicantIrvine Scientific Sales Co., Inc.
Decision Date2002-07-05
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

EMBRYO BIOPSY 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 2002-07-05 under 510(k) number K021358. 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 BIOPSY MEDIUM?

EMBRYO BIOPSY MEDIUM is a medical device that received FDA 510(k) clearance on 2002-07-05. The listed applicant is Irvine Scientific Sales Co., Inc.. The 510(k) number is K021358.

When did EMBRYO BIOPSY MEDIUM receive FDA 510(k) clearance?

EMBRYO BIOPSY MEDIUM received FDA 510(k) clearance on 2002-07-05, under 510(k) number K021358.

Who is the listed applicant for EMBRYO BIOPSY 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 BIOPSY MEDIUM?

The FDA product code for EMBRYO BIOPSY MEDIUM is MQL.

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Related Devices (Code: MQL)

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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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