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FDA 510(k)

AMDEV LYTENING 2 SODIUM/POTASSIUM/LITHIUM/ANALYZER

K-Number: K896692 · 1990-01-02

ApplicantBaxter Healthcare Corp
Decision Date1990-01-02
Product CodeCEM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AMDEV LYTENING 2 SODIUM/POTASSIUM/LITHIUM/ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1990-01-02 under 510(k) number K896692. The device is classified under product code CEM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMDEV LYTENING 2 SODIUM/POTASSIUM/LITHIUM/ANALYZER?

AMDEV LYTENING 2 SODIUM/POTASSIUM/LITHIUM/ANALYZER is a medical device that received FDA 510(k) clearance on 1990-01-02. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K896692.

When did AMDEV LYTENING 2 SODIUM/POTASSIUM/LITHIUM/ANALYZER receive FDA 510(k) clearance?

AMDEV LYTENING 2 SODIUM/POTASSIUM/LITHIUM/ANALYZER received FDA 510(k) clearance on 1990-01-02, under 510(k) number K896692.

Who is the listed applicant for AMDEV LYTENING 2 SODIUM/POTASSIUM/LITHIUM/ANALYZER?

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

What is the FDA product code for AMDEV LYTENING 2 SODIUM/POTASSIUM/LITHIUM/ANALYZER?

The FDA product code for AMDEV LYTENING 2 SODIUM/POTASSIUM/LITHIUM/ANALYZER is CEM.

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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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