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FDA 510(k)

A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES

K-Number: K915300 · 1992-02-18

ApplicantAlto Development Corp.
Decision Date1992-02-18
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES 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 1992-02-18 under 510(k) number K915300. 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 & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES?

A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES is a medical device that received FDA 510(k) clearance on 1992-02-18. The listed applicant is Alto Development Corp.. The 510(k) number is K915300.

When did A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES receive FDA 510(k) clearance?

A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES received FDA 510(k) clearance on 1992-02-18, under 510(k) number K915300.

Who is the listed applicant for A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES?

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 & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES?

The FDA product code for A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES is GEI.

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Other records listing Alto Development Corp. as applicant

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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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