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FDA 510(k)

MEDI-TRACE DISPOSABLE PRESSURE TRANSDUCER

K-Number: K850898 · 1985-07-25

Decision Date1985-07-25
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDI-TRACE DISPOSABLE PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Trace Products Division. It received FDA 510(k) clearance on 1985-07-25 under 510(k) number K850898. 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 MEDI-TRACE DISPOSABLE PRESSURE TRANSDUCER?

MEDI-TRACE DISPOSABLE PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1985-07-25. The listed applicant is Medi-Trace Products Division. The 510(k) number is K850898.

When did MEDI-TRACE DISPOSABLE PRESSURE TRANSDUCER receive FDA 510(k) clearance?

MEDI-TRACE DISPOSABLE PRESSURE TRANSDUCER received FDA 510(k) clearance on 1985-07-25, under 510(k) number K850898.

Who is the listed applicant for MEDI-TRACE DISPOSABLE PRESSURE TRANSDUCER?

The FDA 510(k) record lists Medi-Trace Products Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI-TRACE DISPOSABLE PRESSURE TRANSDUCER?

The FDA product code for MEDI-TRACE DISPOSABLE PRESSURE TRANSDUCER is DRS.

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.

Related Devices (Code: DRS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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