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FDA 510(k)

LEAD, TIMED PACING, IMPLANTABLE

K-Number: K782004 · 1978-12-15

ApplicantDaig Corp.
Decision Date1978-12-15
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LEAD, TIMED PACING, IMPLANTABLE is the device name listed in this FDA 510(k) record. The listed applicant is Daig Corp.. It received FDA 510(k) clearance on 1978-12-15 under 510(k) number K782004. 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 LEAD, TIMED PACING, IMPLANTABLE?

LEAD, TIMED PACING, IMPLANTABLE is a medical device that received FDA 510(k) clearance on 1978-12-15. The listed applicant is Daig Corp.. The 510(k) number is K782004.

When did LEAD, TIMED PACING, IMPLANTABLE receive FDA 510(k) clearance?

LEAD, TIMED PACING, IMPLANTABLE received FDA 510(k) clearance on 1978-12-15, under 510(k) number K782004.

Who is the listed applicant for LEAD, TIMED PACING, IMPLANTABLE?

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 LEAD, TIMED PACING, IMPLANTABLE?

The FDA product code for LEAD, TIMED PACING, IMPLANTABLE 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.

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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

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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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