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FDA 510(k)

ZINC DUST SUSPENSION

K-Number: K842299 · 1984-06-26

Decision Date1984-06-26
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ZINC DUST SUSPENSION is the device name listed in this FDA 510(k) record. The listed applicant is Irvine Diagnostic Services. It received FDA 510(k) clearance on 1984-06-26 under 510(k) number K842299. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZINC DUST SUSPENSION?

ZINC DUST SUSPENSION is a medical device that received FDA 510(k) clearance on 1984-06-26. The listed applicant is Irvine Diagnostic Services. The 510(k) number is K842299.

When did ZINC DUST SUSPENSION receive FDA 510(k) clearance?

ZINC DUST SUSPENSION received FDA 510(k) clearance on 1984-06-26, under 510(k) number K842299.

Who is the listed applicant for ZINC DUST SUSPENSION?

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

What is the FDA product code for ZINC DUST SUSPENSION?

The FDA product code for ZINC DUST SUSPENSION is JSF.

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 Diagnostic Services 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.

View all 10 devices →

Related Devices (Code: JSF)

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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