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FDA 510(k)

THE REUSABLE SPACEMAKER SURGICAL BALLOON DISSECTOR & CANNULA

K-Number: K952278 · 1995-08-07

Decision Date1995-08-07
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

THE REUSABLE SPACEMAKER SURGICAL BALLOON DISSECTOR & CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is General Surgical Innovations. It received FDA 510(k) clearance on 1995-08-07 under 510(k) number K952278. 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 THE REUSABLE SPACEMAKER SURGICAL BALLOON DISSECTOR & CANNULA?

THE REUSABLE SPACEMAKER SURGICAL BALLOON DISSECTOR & CANNULA is a medical device that received FDA 510(k) clearance on 1995-08-07. The listed applicant is General Surgical Innovations. The 510(k) number is K952278.

When did THE REUSABLE SPACEMAKER SURGICAL BALLOON DISSECTOR & CANNULA receive FDA 510(k) clearance?

THE REUSABLE SPACEMAKER SURGICAL BALLOON DISSECTOR & CANNULA received FDA 510(k) clearance on 1995-08-07, under 510(k) number K952278.

Who is the listed applicant for THE REUSABLE SPACEMAKER SURGICAL BALLOON DISSECTOR & CANNULA?

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

What is the FDA product code for THE REUSABLE SPACEMAKER SURGICAL BALLOON DISSECTOR & CANNULA?

The FDA product code for THE REUSABLE SPACEMAKER SURGICAL BALLOON DISSECTOR & CANNULA 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 General Surgical Innovations 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 14 devices →

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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