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FDA 510(k)

USCI TRANSTHORACIC TEMP. PACING ELECTROD

K-Number: K812307 · 1981-09-21

Decision Date1981-09-21
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

USCI TRANSTHORACIC TEMP. PACING ELECTROD is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1981-09-21 under 510(k) number K812307. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USCI TRANSTHORACIC TEMP. PACING ELECTROD?

USCI TRANSTHORACIC TEMP. PACING ELECTROD is a medical device that received FDA 510(k) clearance on 1981-09-21. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K812307.

When did USCI TRANSTHORACIC TEMP. PACING ELECTROD receive FDA 510(k) clearance?

USCI TRANSTHORACIC TEMP. PACING ELECTROD received FDA 510(k) clearance on 1981-09-21, under 510(k) number K812307.

Who is the listed applicant for USCI TRANSTHORACIC TEMP. PACING ELECTROD?

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

What is the FDA product code for USCI TRANSTHORACIC TEMP. PACING ELECTROD?

The FDA product code for USCI TRANSTHORACIC TEMP. PACING ELECTROD is LDF.

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 C.R. Bard, 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 616 devices →

Related Devices (Code: LDF)

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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