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FDA 510(k)

METRICIDE 28

K-Number: K931052 · 1994-12-06

Decision Date1994-12-06
Product CodeMED
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

METRICIDE 28 is the device name listed in this FDA 510(k) record. The listed applicant is Metrex Research Corp.. It received FDA 510(k) clearance on 1994-12-06 under 510(k) number K931052. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METRICIDE 28?

METRICIDE 28 is a medical device that received FDA 510(k) clearance on 1994-12-06. The listed applicant is Metrex Research Corp.. The 510(k) number is K931052.

When did METRICIDE 28 receive FDA 510(k) clearance?

METRICIDE 28 received FDA 510(k) clearance on 1994-12-06, under 510(k) number K931052.

Who is the listed applicant for METRICIDE 28?

The FDA 510(k) record lists Metrex Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for METRICIDE 28?

The FDA product code for METRICIDE 28 is MED.

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 Metrex Research Corp. 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.

Related Devices (Code: MED)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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