FDA 510(k)

MINOLTA/MARQUEST PULSOX-7 OXYGEN SATURATION MONIT.

K-Number: K863918 · 1987-01-07

ApplicantMarquest Medical Products, Inc.

Decision Date1987-01-07

Product CodeDQA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MINOLTA/MARQUEST PULSOX-7 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 1987-01-07 under 510(k) number K863918. 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/MARQUEST PULSOX-7 OXYGEN SATURATION MONIT.?

MINOLTA/MARQUEST PULSOX-7 OXYGEN SATURATION MONIT. is a medical device that received FDA 510(k) clearance on 1987-01-07. The listed applicant is Marquest Medical Products, Inc.. The 510(k) number is K863918.

When did MINOLTA/MARQUEST PULSOX-7 OXYGEN SATURATION MONIT. receive FDA 510(k) clearance?

MINOLTA/MARQUEST PULSOX-7 OXYGEN SATURATION MONIT. received FDA 510(k) clearance on 1987-01-07, under 510(k) number K863918.

Who is the listed applicant for MINOLTA/MARQUEST PULSOX-7 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/MARQUEST PULSOX-7 OXYGEN SATURATION MONIT.?

The FDA product code for MINOLTA/MARQUEST PULSOX-7 OXYGEN SATURATION MONIT. is DQA.

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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.