INTERCEPTOR, 662-01
K-Number: K844279 · 1985-01-24
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Device Summary
Frequently Asked Questions
What is the INTERCEPTOR, 662-01?
INTERCEPTOR, 662-01 is a medical device that received FDA 510(k) clearance on 1985-01-24. The listed applicant is Intermedics, Inc.. The 510(k) number is K844279.
When did INTERCEPTOR, 662-01 receive FDA 510(k) clearance?
INTERCEPTOR, 662-01 received FDA 510(k) clearance on 1985-01-24, under 510(k) number K844279.
Who is the listed applicant for INTERCEPTOR, 662-01?
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 INTERCEPTOR, 662-01?
The FDA product code for INTERCEPTOR, 662-01 is GZJ.
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: GZJ)
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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