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FDA 510(k)

AMINO ACID ANALYSER SYSTEM

K-Number: K803004 · 1980-12-22

ApplicantLkb Instruments, Inc.
Decision Date1980-12-22
Product CodeJJF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AMINO ACID ANALYSER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Lkb Instruments, Inc.. It received FDA 510(k) clearance on 1980-12-22 under 510(k) number K803004. The device is classified under product code JJF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMINO ACID ANALYSER SYSTEM?

AMINO ACID ANALYSER SYSTEM is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K803004.

When did AMINO ACID ANALYSER SYSTEM receive FDA 510(k) clearance?

AMINO ACID ANALYSER SYSTEM received FDA 510(k) clearance on 1980-12-22, under 510(k) number K803004.

Who is the listed applicant for AMINO ACID ANALYSER SYSTEM?

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

What is the FDA product code for AMINO ACID ANALYSER SYSTEM?

The FDA product code for AMINO ACID ANALYSER SYSTEM is JJF.

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Other records listing Lkb Instruments, Inc. as applicant

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Related Devices (Code: JJF)

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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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