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FDA 510(k)

EZX YELLOW, BLUE OR ORANGE

K-Number: K852170 · 1985-09-05

Decision Date1985-09-05
Product CodeEGZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EZX YELLOW, BLUE OR ORANGE is the device name listed in this FDA 510(k) record. The listed applicant is Strong Marketing. It received FDA 510(k) clearance on 1985-09-05 under 510(k) number K852170. The device is classified under product code EGZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZX YELLOW, BLUE OR ORANGE?

EZX YELLOW, BLUE OR ORANGE is a medical device that received FDA 510(k) clearance on 1985-09-05. The listed applicant is Strong Marketing. The 510(k) number is K852170.

When did EZX YELLOW, BLUE OR ORANGE receive FDA 510(k) clearance?

EZX YELLOW, BLUE OR ORANGE received FDA 510(k) clearance on 1985-09-05, under 510(k) number K852170.

Who is the listed applicant for EZX YELLOW, BLUE OR ORANGE?

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

What is the FDA product code for EZX YELLOW, BLUE OR ORANGE?

The FDA product code for EZX YELLOW, BLUE OR ORANGE is EGZ.

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.

Related Devices (Code: EGZ)

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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