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FDA 510(k)

LYOPHILIZED MULTIBLAST MEDIUM KIT

K-Number: K072608 · 2008-01-30

ApplicantIrvine Scientific Sales Co., Inc.
Decision Date2008-01-30
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LYOPHILIZED MULTIBLAST MEDIUM KIT 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 2008-01-30 under 510(k) number K072608. 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 LYOPHILIZED MULTIBLAST MEDIUM KIT?

LYOPHILIZED MULTIBLAST MEDIUM KIT is a medical device that received FDA 510(k) clearance on 2008-01-30. The listed applicant is Irvine Scientific Sales Co., Inc.. The 510(k) number is K072608.

When did LYOPHILIZED MULTIBLAST MEDIUM KIT receive FDA 510(k) clearance?

LYOPHILIZED MULTIBLAST MEDIUM KIT received FDA 510(k) clearance on 2008-01-30, under 510(k) number K072608.

Who is the listed applicant for LYOPHILIZED MULTIBLAST MEDIUM KIT?

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 LYOPHILIZED MULTIBLAST MEDIUM KIT?

The FDA product code for LYOPHILIZED MULTIBLAST MEDIUM KIT 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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