Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

I.L. MODEL 643 FLAME PHOTOMETER

K-Number: K771337 · 1977-10-18

Decision Date1977-10-18
Product CodeJJO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

I.L. MODEL 643 FLAME PHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1977-10-18 under 510(k) number K771337. 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 I.L. MODEL 643 FLAME PHOTOMETER?

I.L. MODEL 643 FLAME PHOTOMETER is a medical device that received FDA 510(k) clearance on 1977-10-18. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K771337.

When did I.L. MODEL 643 FLAME PHOTOMETER receive FDA 510(k) clearance?

I.L. MODEL 643 FLAME PHOTOMETER received FDA 510(k) clearance on 1977-10-18, under 510(k) number K771337.

Who is the listed applicant for I.L. MODEL 643 FLAME PHOTOMETER?

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

What is the FDA product code for I.L. MODEL 643 FLAME PHOTOMETER?

The FDA product code for I.L. MODEL 643 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 Instrumentation Laboratory CO 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 315 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.

↑