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)

IE MAGNETIC EXTRACTOR

K-Number: K904668 · 1991-03-21

ApplicantOlympus Corp.
Decision Date1991-03-21
Product CodeFCC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

IE MAGNETIC EXTRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1991-03-21 under 510(k) number K904668. The device is classified under product code FCC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IE MAGNETIC EXTRACTOR?

IE MAGNETIC EXTRACTOR is a medical device that received FDA 510(k) clearance on 1991-03-21. The listed applicant is Olympus Corp.. The 510(k) number is K904668.

When did IE MAGNETIC EXTRACTOR receive FDA 510(k) clearance?

IE MAGNETIC EXTRACTOR received FDA 510(k) clearance on 1991-03-21, under 510(k) number K904668.

Who is the listed applicant for IE MAGNETIC EXTRACTOR?

The FDA 510(k) record lists Olympus Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IE MAGNETIC EXTRACTOR?

The FDA product code for IE MAGNETIC EXTRACTOR is FCC.

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 Olympus Corp. 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 142 devices →

Related Devices (Code: FCC)

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.

↑