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FDA 510(k)

MULTIPURPOSE HANDLING MEDIUM

K-Number: K121128 · 2012-06-06

Decision Date2012-06-06
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MULTIPURPOSE HANDLING 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 2012-06-06 under 510(k) number K121128. 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 MULTIPURPOSE HANDLING MEDIUM?

MULTIPURPOSE HANDLING MEDIUM is a medical device that received FDA 510(k) clearance on 2012-06-06. The listed applicant is Irvine Scientific Sales Co., Inc.. The 510(k) number is K121128.

When did MULTIPURPOSE HANDLING MEDIUM receive FDA 510(k) clearance?

MULTIPURPOSE HANDLING MEDIUM received FDA 510(k) clearance on 2012-06-06, under 510(k) number K121128.

Who is the listed applicant for MULTIPURPOSE HANDLING 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 MULTIPURPOSE HANDLING MEDIUM?

The FDA product code for MULTIPURPOSE HANDLING MEDIUM is MQL.

Related Clinical Trials

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.

Other records listing Irvine Scientific Sales Co., 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.

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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.

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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