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FDA 510(k)

MINIOX V PULSE OXIMETER

K-Number: K905310 · 1991-05-28

Decision Date1991-05-28
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINIOX V PULSE OXIMETER 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 1991-05-28 under 510(k) number K905310. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIOX V PULSE OXIMETER?

MINIOX V PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1991-05-28. The listed applicant is Catalyst Research Corp.. The 510(k) number is K905310.

When did MINIOX V PULSE OXIMETER receive FDA 510(k) clearance?

MINIOX V PULSE OXIMETER received FDA 510(k) clearance on 1991-05-28, under 510(k) number K905310.

Who is the listed applicant for MINIOX V PULSE OXIMETER?

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 MINIOX V PULSE OXIMETER?

The FDA product code for MINIOX V PULSE OXIMETER is DQA.

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: DQA)

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

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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