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FDA 510(k)

QUANTUM MONO-POLAR ELECTROSURGICAL CABLE

K-Number: K941908 · 1994-05-23

Decision Date1994-05-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

QUANTUM MONO-POLAR ELECTROSURGICAL CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Quantum Instruments Corp.. It received FDA 510(k) clearance on 1994-05-23 under 510(k) number K941908. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTUM MONO-POLAR ELECTROSURGICAL CABLE?

QUANTUM MONO-POLAR ELECTROSURGICAL CABLE is a medical device that received FDA 510(k) clearance on 1994-05-23. The listed applicant is Quantum Instruments Corp.. The 510(k) number is K941908.

When did QUANTUM MONO-POLAR ELECTROSURGICAL CABLE receive FDA 510(k) clearance?

QUANTUM MONO-POLAR ELECTROSURGICAL CABLE received FDA 510(k) clearance on 1994-05-23, under 510(k) number K941908.

Who is the listed applicant for QUANTUM MONO-POLAR ELECTROSURGICAL CABLE?

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

What is the FDA product code for QUANTUM MONO-POLAR ELECTROSURGICAL CABLE?

The FDA product code for QUANTUM MONO-POLAR ELECTROSURGICAL CABLE is GEI.

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 Quantum Instruments 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.

Related Devices (Code: GEI)

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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