MODEL KY PACEMAKER LEAD - VARIOUS
K-Number: K823891 · 1983-03-31
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Device Summary
Frequently Asked Questions
What is the MODEL KY PACEMAKER LEAD - VARIOUS?
MODEL KY PACEMAKER LEAD - VARIOUS is a medical device that received FDA 510(k) clearance on 1983-03-31. The listed applicant is Oscor, Inc.. The 510(k) number is K823891.
When did MODEL KY PACEMAKER LEAD - VARIOUS receive FDA 510(k) clearance?
MODEL KY PACEMAKER LEAD - VARIOUS received FDA 510(k) clearance on 1983-03-31, under 510(k) number K823891.
Who is the listed applicant for MODEL KY PACEMAKER LEAD - VARIOUS?
The FDA 510(k) record lists Oscor, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL KY PACEMAKER LEAD - VARIOUS?
The FDA product code for MODEL KY PACEMAKER LEAD - VARIOUS 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 Oscor, 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: 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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