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FDA 510(k)

ELVI 655 FLAME PHOTOMETER

K-Number: K843375 · 1985-05-20

Decision Date1985-05-20
Product CodeJJO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELVI 655 FLAME PHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Logos Scientific, Inc.. It received FDA 510(k) clearance on 1985-05-20 under 510(k) number K843375. The device is classified under product code JJO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELVI 655 FLAME PHOTOMETER?

ELVI 655 FLAME PHOTOMETER is a medical device that received FDA 510(k) clearance on 1985-05-20. The listed applicant is Logos Scientific, Inc.. The 510(k) number is K843375.

When did ELVI 655 FLAME PHOTOMETER receive FDA 510(k) clearance?

ELVI 655 FLAME PHOTOMETER received FDA 510(k) clearance on 1985-05-20, under 510(k) number K843375.

Who is the listed applicant for ELVI 655 FLAME PHOTOMETER?

The FDA 510(k) record lists Logos Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELVI 655 FLAME PHOTOMETER?

The FDA product code for ELVI 655 FLAME PHOTOMETER is JJO.

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 Logos Scientific, 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.

View all 9 devices →

Related Devices (Code: JJO)

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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