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FDA 510(k)

UNIPOLAR LEAD CONFIGURATION CONDUCTOR

K-Number: K800348 · 1980-05-28

ApplicantDaig Corp.
Decision Date1980-05-28
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

UNIPOLAR LEAD CONFIGURATION CONDUCTOR is the device name listed in this FDA 510(k) record. The listed applicant is Daig Corp.. It received FDA 510(k) clearance on 1980-05-28 under 510(k) number K800348. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIPOLAR LEAD CONFIGURATION CONDUCTOR?

UNIPOLAR LEAD CONFIGURATION CONDUCTOR is a medical device that received FDA 510(k) clearance on 1980-05-28. The listed applicant is Daig Corp.. The 510(k) number is K800348.

When did UNIPOLAR LEAD CONFIGURATION CONDUCTOR receive FDA 510(k) clearance?

UNIPOLAR LEAD CONFIGURATION CONDUCTOR received FDA 510(k) clearance on 1980-05-28, under 510(k) number K800348.

Who is the listed applicant for UNIPOLAR LEAD CONFIGURATION CONDUCTOR?

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

What is the FDA product code for UNIPOLAR LEAD CONFIGURATION CONDUCTOR?

The FDA product code for UNIPOLAR LEAD CONFIGURATION CONDUCTOR is DTB.

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 Daig Corp. 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 63 devices →

Related Devices (Code: DTB)

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

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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