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FDA 510(k)

CLA 200 CHEMPRO(R) LIPID ANALYZER

K-Number: K892238 · 1989-06-07

Decision Date1989-06-07
Product CodeCHH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CLA 200 CHEMPRO(R) LIPID ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1989-06-07 under 510(k) number K892238. The device is classified under product code CHH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLA 200 CHEMPRO(R) LIPID ANALYZER?

CLA 200 CHEMPRO(R) LIPID ANALYZER is a medical device that received FDA 510(k) clearance on 1989-06-07. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K892238.

When did CLA 200 CHEMPRO(R) LIPID ANALYZER receive FDA 510(k) clearance?

CLA 200 CHEMPRO(R) LIPID ANALYZER received FDA 510(k) clearance on 1989-06-07, under 510(k) number K892238.

Who is the listed applicant for CLA 200 CHEMPRO(R) LIPID ANALYZER?

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

What is the FDA product code for CLA 200 CHEMPRO(R) LIPID ANALYZER?

The FDA product code for CLA 200 CHEMPRO(R) LIPID ANALYZER is CHH.

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 Johnson & Johnson Professionals, Inc. 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 206 devices →

Related Devices (Code: CHH)

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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