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FDA 510(k)

MINICO

K-Number: K781746 · 1978-12-05

ApplicantCatalyst Research Corp.
Decision Date1978-12-05
Product CodeCCJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MINICO 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 1978-12-05 under 510(k) number K781746. The device is classified under product code CCJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINICO?

MINICO is a medical device that received FDA 510(k) clearance on 1978-12-05. The listed applicant is Catalyst Research Corp.. The 510(k) number is K781746.

When did MINICO receive FDA 510(k) clearance?

MINICO received FDA 510(k) clearance on 1978-12-05, under 510(k) number K781746.

Who is the listed applicant for MINICO?

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 MINICO?

The FDA product code for MINICO is CCJ.

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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.

K905310MINIOX V PULSE OXIMETERK874132MINIOX IV PORTABLE PULSE OXIMETERK862798MINIOX 100 PULSE OXIMETERK833995MINI OX IIK833326MINI OX III OXYGEN MONITORK790784MODEL M25R, OXYGEN ANALYZER

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Related Devices (Code: CCJ)

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.

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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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