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FDA 510(k)

MX900-DPT, DISPOSABLE PRESSURE TRANSDUCER

K-Number: K870301 · 1987-05-06

ApplicantMedex, Inc.
Decision Date1987-05-06
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MX900-DPT, DISPOSABLE PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1987-05-06 under 510(k) number K870301. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MX900-DPT, DISPOSABLE PRESSURE TRANSDUCER?

MX900-DPT, DISPOSABLE PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1987-05-06. The listed applicant is Medex, Inc.. The 510(k) number is K870301.

When did MX900-DPT, DISPOSABLE PRESSURE TRANSDUCER receive FDA 510(k) clearance?

MX900-DPT, DISPOSABLE PRESSURE TRANSDUCER received FDA 510(k) clearance on 1987-05-06, under 510(k) number K870301.

Who is the listed applicant for MX900-DPT, DISPOSABLE PRESSURE TRANSDUCER?

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

What is the FDA product code for MX900-DPT, DISPOSABLE PRESSURE TRANSDUCER?

The FDA product code for MX900-DPT, DISPOSABLE PRESSURE TRANSDUCER is DRS.

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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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