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FDA 510(k)

A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS

K-Number: K930528 · 1993-05-17

ApplicantAlto Development Corp.
Decision Date1993-05-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS is the device name listed in this FDA 510(k) record. The listed applicant is Alto Development Corp.. It received FDA 510(k) clearance on 1993-05-17 under 510(k) number K930528. 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 A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS?

A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS is a medical device that received FDA 510(k) clearance on 1993-05-17. The listed applicant is Alto Development Corp.. The 510(k) number is K930528.

When did A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS receive FDA 510(k) clearance?

A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS received FDA 510(k) clearance on 1993-05-17, under 510(k) number K930528.

Who is the listed applicant for A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS?

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

What is the FDA product code for A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS?

The FDA product code for A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS is GEI.

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Other records listing Alto Development 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: GEI)

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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.

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