ELECTRODE LEAD MODEL 030-198
K-Number: K782097 · 1978-12-22
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Device Summary
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.
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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