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FDA 510(k)

AMPULED FLAME PHOTOMETER STANDARDS

K-Number: K810618 · 1981-03-31

ApplicantUnited Diagnostics, Inc.
Decision Date1981-03-31
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AMPULED FLAME PHOTOMETER STANDARDS is the device name listed in this FDA 510(k) record. The listed applicant is United Diagnostics, Inc.. It received FDA 510(k) clearance on 1981-03-31 under 510(k) number K810618. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMPULED FLAME PHOTOMETER STANDARDS?

AMPULED FLAME PHOTOMETER STANDARDS is a medical device that received FDA 510(k) clearance on 1981-03-31. The listed applicant is United Diagnostics, Inc.. The 510(k) number is K810618.

When did AMPULED FLAME PHOTOMETER STANDARDS receive FDA 510(k) clearance?

AMPULED FLAME PHOTOMETER STANDARDS received FDA 510(k) clearance on 1981-03-31, under 510(k) number K810618.

Who is the listed applicant for AMPULED FLAME PHOTOMETER STANDARDS?

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

What is the FDA product code for AMPULED FLAME PHOTOMETER STANDARDS?

The FDA product code for AMPULED FLAME PHOTOMETER STANDARDS is JIS.

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Other records listing United Diagnostics, Inc. as applicant

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Related Devices (Code: JIS)

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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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