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FDA 510(k)

SAMPLE IDENTIFICATION STATION MODEL 38010

K-Number: K884269 · 1989-01-09

Decision Date1989-01-09
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SAMPLE IDENTIFICATION STATION MODEL 38010 is the device name listed in this FDA 510(k) record. The listed applicant is Icn Micromedic Systems. It received FDA 510(k) clearance on 1989-01-09 under 510(k) number K884269. The device is classified under product code JJJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAMPLE IDENTIFICATION STATION MODEL 38010?

SAMPLE IDENTIFICATION STATION MODEL 38010 is a medical device that received FDA 510(k) clearance on 1989-01-09. The listed applicant is Icn Micromedic Systems. The 510(k) number is K884269.

When did SAMPLE IDENTIFICATION STATION MODEL 38010 receive FDA 510(k) clearance?

SAMPLE IDENTIFICATION STATION MODEL 38010 received FDA 510(k) clearance on 1989-01-09, under 510(k) number K884269.

Who is the listed applicant for SAMPLE IDENTIFICATION STATION MODEL 38010?

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

What is the FDA product code for SAMPLE IDENTIFICATION STATION MODEL 38010?

The FDA product code for SAMPLE IDENTIFICATION STATION MODEL 38010 is JJJ.

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 Icn Micromedic Systems 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: JJJ)

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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