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FDA 510(k)

MODEL M25RL, (CRC) OXYGEN ANALYZER

K-Number: K790785 · 1979-04-27

Decision Date1979-04-27
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL M25RL, (CRC) OXYGEN ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Catalyst Research Corp.. It received FDA 510(k) clearance on 1979-04-27 under 510(k) number K790785. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL M25RL, (CRC) OXYGEN ANALYZER?

MODEL M25RL, (CRC) OXYGEN ANALYZER is a medical device that received FDA 510(k) clearance on 1979-04-27. The listed applicant is Catalyst Research Corp.. The 510(k) number is K790785.

When did MODEL M25RL, (CRC) OXYGEN ANALYZER receive FDA 510(k) clearance?

MODEL M25RL, (CRC) OXYGEN ANALYZER received FDA 510(k) clearance on 1979-04-27, under 510(k) number K790785.

Who is the listed applicant for MODEL M25RL, (CRC) OXYGEN ANALYZER?

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

What is the FDA product code for MODEL M25RL, (CRC) OXYGEN ANALYZER?

The FDA product code for MODEL M25RL, (CRC) OXYGEN ANALYZER is CCL.

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 Catalyst Research Corp. 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 9 devices →

Related Devices (Code: CCL)

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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