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FDA 510(k)

NARCO TELECARE PRESSURE TRANSDUCER DOME

K-Number: K812884 · 1981-11-02

Decision Date1981-11-02
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NARCO TELECARE PRESSURE TRANSDUCER DOME is the device name listed in this FDA 510(k) record. The listed applicant is Narco Scientific. It received FDA 510(k) clearance on 1981-11-02 under 510(k) number K812884. 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 NARCO TELECARE PRESSURE TRANSDUCER DOME?

NARCO TELECARE PRESSURE TRANSDUCER DOME is a medical device that received FDA 510(k) clearance on 1981-11-02. The listed applicant is Narco Scientific. The 510(k) number is K812884.

When did NARCO TELECARE PRESSURE TRANSDUCER DOME receive FDA 510(k) clearance?

NARCO TELECARE PRESSURE TRANSDUCER DOME received FDA 510(k) clearance on 1981-11-02, under 510(k) number K812884.

Who is the listed applicant for NARCO TELECARE PRESSURE TRANSDUCER DOME?

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

What is the FDA product code for NARCO TELECARE PRESSURE TRANSDUCER DOME?

The FDA product code for NARCO TELECARE PRESSURE TRANSDUCER DOME 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 Narco Scientific 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.

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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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