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FDA 510(k)

EURAMARK 610 PHOTOMETER

K-Number: K903164 · 1990-08-09

Decision Date1990-08-09
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EURAMARK 610 PHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Euro-American Marketing Group, Inc.. It received FDA 510(k) clearance on 1990-08-09 under 510(k) number K903164. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EURAMARK 610 PHOTOMETER?

EURAMARK 610 PHOTOMETER is a medical device that received FDA 510(k) clearance on 1990-08-09. The listed applicant is Euro-American Marketing Group, Inc.. The 510(k) number is K903164.

When did EURAMARK 610 PHOTOMETER receive FDA 510(k) clearance?

EURAMARK 610 PHOTOMETER received FDA 510(k) clearance on 1990-08-09, under 510(k) number K903164.

Who is the listed applicant for EURAMARK 610 PHOTOMETER?

The FDA 510(k) record lists Euro-American Marketing Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EURAMARK 610 PHOTOMETER?

The FDA product code for EURAMARK 610 PHOTOMETER is JJQ.

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 Euro-American Marketing Group, Inc. 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: JJQ)

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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