Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INTERCEPTOR, 662-01

K-Number: K844279 · 1985-01-24

Decision Date1985-01-24
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

INTERCEPTOR, 662-01 is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics, Inc.. It received FDA 510(k) clearance on 1985-01-24 under 510(k) number K844279. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 211 devices →

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.

↑