MODEL 483-06 POLYFLEX IMPLANTABLE PACING LEAD
K-Number: K851457 · 1985-07-11
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Device Summary
Frequently Asked Questions
What is the MODEL 483-06 POLYFLEX IMPLANTABLE PACING LEAD?
MODEL 483-06 POLYFLEX IMPLANTABLE PACING LEAD is a medical device that received FDA 510(k) clearance on 1985-07-11. The listed applicant is Intermedics, Inc.. The 510(k) number is K851457.
When did MODEL 483-06 POLYFLEX IMPLANTABLE PACING LEAD receive FDA 510(k) clearance?
MODEL 483-06 POLYFLEX IMPLANTABLE PACING LEAD received FDA 510(k) clearance on 1985-07-11, under 510(k) number K851457.
Who is the listed applicant for MODEL 483-06 POLYFLEX IMPLANTABLE PACING LEAD?
The FDA 510(k) record lists Intermedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 483-06 POLYFLEX IMPLANTABLE PACING LEAD?
The FDA product code for MODEL 483-06 POLYFLEX IMPLANTABLE PACING LEAD 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 Intermedics, 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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