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FDA 510(k)

TROPHON CHEMICAL INDICATOR

K-Number: K103126 · 2011-03-03

Decision Date2011-03-03
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TROPHON CHEMICAL INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Nanosonics Limited. It received FDA 510(k) clearance on 2011-03-03 under 510(k) number K103126. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROPHON CHEMICAL INDICATOR?

TROPHON CHEMICAL INDICATOR is a medical device that received FDA 510(k) clearance on 2011-03-03. The listed applicant is Nanosonics Limited. The 510(k) number is K103126.

When did TROPHON CHEMICAL INDICATOR receive FDA 510(k) clearance?

TROPHON CHEMICAL INDICATOR received FDA 510(k) clearance on 2011-03-03, under 510(k) number K103126.

Who is the listed applicant for TROPHON CHEMICAL INDICATOR?

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

What is the FDA product code for TROPHON CHEMICAL INDICATOR?

The FDA product code for TROPHON CHEMICAL INDICATOR is JOJ.

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 Nanosonics Limited 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: JOJ)

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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