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)

QUANTUM BI-POLAR ELECTROSURGICAL CABLE

K-Number: K942194 · 1994-05-23

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

Device Summary

QUANTUM BI-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 K942194. 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 BI-POLAR ELECTROSURGICAL CABLE?

QUANTUM BI-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 K942194.

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

QUANTUM BI-POLAR ELECTROSURGICAL CABLE received FDA 510(k) clearance on 1994-05-23, under 510(k) number K942194.

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

The FDA product code for QUANTUM BI-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

View on FDA Database →

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

↑