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FDA 510(k)

MICROWAVE INSURG INTRODUCER

K-Number: K933985 · 1993-11-12

Decision Date1993-11-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MICROWAVE INSURG INTRODUCER is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1993-11-12 under 510(k) number K933985. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROWAVE INSURG INTRODUCER?

MICROWAVE INSURG INTRODUCER is a medical device that received FDA 510(k) clearance on 1993-11-12. The listed applicant is Boston Scientific Corp. The 510(k) number is K933985.

When did MICROWAVE INSURG INTRODUCER receive FDA 510(k) clearance?

MICROWAVE INSURG INTRODUCER received FDA 510(k) clearance on 1993-11-12, under 510(k) number K933985.

Who is the listed applicant for MICROWAVE INSURG INTRODUCER?

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

What is the FDA product code for MICROWAVE INSURG INTRODUCER?

The FDA product code for MICROWAVE INSURG INTRODUCER is GCJ.

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 Boston Scientific 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.

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Related Devices (Code: GCJ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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