IMPLANTABLE PACING LEAD MODELS 487-06 TO 430-01
K-Number: K871580 · 1987-05-22
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Device Summary
Frequently Asked Questions
What is the IMPLANTABLE PACING LEAD MODELS 487-06 TO 430-01?
IMPLANTABLE PACING LEAD MODELS 487-06 TO 430-01 is a medical device that received FDA 510(k) clearance on 1987-05-22. The listed applicant is Intermedics, Inc.. The 510(k) number is K871580.
When did IMPLANTABLE PACING LEAD MODELS 487-06 TO 430-01 receive FDA 510(k) clearance?
IMPLANTABLE PACING LEAD MODELS 487-06 TO 430-01 received FDA 510(k) clearance on 1987-05-22, under 510(k) number K871580.
Who is the listed applicant for IMPLANTABLE PACING LEAD MODELS 487-06 TO 430-01?
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 IMPLANTABLE PACING LEAD MODELS 487-06 TO 430-01?
The FDA product code for IMPLANTABLE PACING LEAD MODELS 487-06 TO 430-01 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 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: 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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