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FDA 510(k)

340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER

K-Number: K945408 · 1995-02-22

Decision Date1995-02-22
Product CodeCHJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Catachem, Inc.. It received FDA 510(k) clearance on 1995-02-22 under 510(k) number K945408. The device is classified under product code CHJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER?

340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER is a medical device that received FDA 510(k) clearance on 1995-02-22. The listed applicant is Catachem, Inc.. The 510(k) number is K945408.

When did 340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER receive FDA 510(k) clearance?

340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER received FDA 510(k) clearance on 1995-02-22, under 510(k) number K945408.

Who is the listed applicant for 340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER?

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

What is the FDA product code for 340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER?

The FDA product code for 340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER is CHJ.

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 Catachem, 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 41 devices →

Related Devices (Code: CHJ)

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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