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FDA 510(k)

MINOLTA SM-32 OXYGEN SATURATION MONIT

K-Number: K833973 · 1984-05-09

ApplicantMarquest Medical Products, Inc.
Decision Date1984-05-09
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINOLTA SM-32 OXYGEN SATURATION MONIT is the device name listed in this FDA 510(k) record. The listed applicant is Marquest Medical Products, Inc.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K833973. 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 MINOLTA SM-32 OXYGEN SATURATION MONIT?

MINOLTA SM-32 OXYGEN SATURATION MONIT is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Marquest Medical Products, Inc.. The 510(k) number is K833973.

When did MINOLTA SM-32 OXYGEN SATURATION MONIT receive FDA 510(k) clearance?

MINOLTA SM-32 OXYGEN SATURATION MONIT received FDA 510(k) clearance on 1984-05-09, under 510(k) number K833973.

Who is the listed applicant for MINOLTA SM-32 OXYGEN SATURATION MONIT?

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

What is the FDA product code for MINOLTA SM-32 OXYGEN SATURATION MONIT?

The FDA product code for MINOLTA SM-32 OXYGEN SATURATION MONIT is DQA.

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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.

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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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