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FDA 510(k)

ELECTRODE LEAD MODEL 030-198

K-Number: K782097 · 1978-12-22

Decision Date1978-12-22
Product CodeDTD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRODE LEAD MODEL 030-198 is the device name listed in this FDA 510(k) record. The listed applicant is Telectronics, Inc.. It received FDA 510(k) clearance on 1978-12-22 under 510(k) number K782097. The device is classified under product code DTD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRODE LEAD MODEL 030-198?

ELECTRODE LEAD MODEL 030-198 is a medical device that received FDA 510(k) clearance on 1978-12-22. The listed applicant is Telectronics, Inc.. The 510(k) number is K782097.

When did ELECTRODE LEAD MODEL 030-198 receive FDA 510(k) clearance?

ELECTRODE LEAD MODEL 030-198 received FDA 510(k) clearance on 1978-12-22, under 510(k) number K782097.

Who is the listed applicant for ELECTRODE LEAD MODEL 030-198?

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

What is the FDA product code for ELECTRODE LEAD MODEL 030-198?

The FDA product code for ELECTRODE LEAD MODEL 030-198 is DTD.

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 Telectronics, 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 107 devices →

Related Devices (Code: DTD)

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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