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FDA 510(k)

MULTIBLAST MEDIUM

K-Number: K034063 · 2004-04-26

ApplicantIrvine Scientific Sales Co., Inc.
Decision Date2004-04-26
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MULTIBLAST 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 2004-04-26 under 510(k) number K034063. 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 MULTIBLAST MEDIUM?

MULTIBLAST MEDIUM is a medical device that received FDA 510(k) clearance on 2004-04-26. The listed applicant is Irvine Scientific Sales Co., Inc.. The 510(k) number is K034063.

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

MULTIBLAST MEDIUM received FDA 510(k) clearance on 2004-04-26, under 510(k) number K034063.

Who is the listed applicant for MULTIBLAST 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 MULTIBLAST MEDIUM?

The FDA product code for MULTIBLAST 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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