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FDA 510(k)

MERITRANS(TM) DISPOSABLE TRANSDUCER

K-Number: K920977 · 1992-12-11

Decision Date1992-12-11
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MERITRANS(TM) DISPOSABLE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 1992-12-11 under 510(k) number K920977. 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 MERITRANS(TM) DISPOSABLE TRANSDUCER?

MERITRANS(TM) DISPOSABLE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1992-12-11. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K920977.

When did MERITRANS(TM) DISPOSABLE TRANSDUCER receive FDA 510(k) clearance?

MERITRANS(TM) DISPOSABLE TRANSDUCER received FDA 510(k) clearance on 1992-12-11, under 510(k) number K920977.

Who is the listed applicant for MERITRANS(TM) DISPOSABLE TRANSDUCER?

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

What is the FDA product code for MERITRANS(TM) DISPOSABLE TRANSDUCER?

The FDA product code for MERITRANS(TM) DISPOSABLE 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.

Other records listing Merit Medical Systems, Inc. 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 159 devices →

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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