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FDA 510(k)

PARALLEL FLAME PHOTOMETER & SODIUM

K-Number: K834248 · 1984-01-30

Decision Date1984-01-30
Product CodeJGT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PARALLEL FLAME PHOTOMETER & SODIUM is the device name listed in this FDA 510(k) record. The listed applicant is American Monitor Corp.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K834248. The device is classified under product code JGT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARALLEL FLAME PHOTOMETER & SODIUM?

PARALLEL FLAME PHOTOMETER & SODIUM is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is American Monitor Corp.. The 510(k) number is K834248.

When did PARALLEL FLAME PHOTOMETER & SODIUM receive FDA 510(k) clearance?

PARALLEL FLAME PHOTOMETER & SODIUM received FDA 510(k) clearance on 1984-01-30, under 510(k) number K834248.

Who is the listed applicant for PARALLEL FLAME PHOTOMETER & SODIUM?

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

What is the FDA product code for PARALLEL FLAME PHOTOMETER & SODIUM?

The FDA product code for PARALLEL FLAME PHOTOMETER & SODIUM is JGT.

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 American Monitor Corp. 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 73 devices →

Related Devices (Code: JGT)

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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