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FDA 510(k)

ASPEN SURGICAL SYSTEMS ACCESSORY ELECTRODE

K-Number: K943542 · 1994-09-01

ApplicantConmedcorp
Decision Date1994-09-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ASPEN SURGICAL SYSTEMS ACCESSORY ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1994-09-01 under 510(k) number K943542. 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 ASPEN SURGICAL SYSTEMS ACCESSORY ELECTRODE?

ASPEN SURGICAL SYSTEMS ACCESSORY ELECTRODE is a medical device that received FDA 510(k) clearance on 1994-09-01. The listed applicant is Conmedcorp. The 510(k) number is K943542.

When did ASPEN SURGICAL SYSTEMS ACCESSORY ELECTRODE receive FDA 510(k) clearance?

ASPEN SURGICAL SYSTEMS ACCESSORY ELECTRODE received FDA 510(k) clearance on 1994-09-01, under 510(k) number K943542.

Who is the listed applicant for ASPEN SURGICAL SYSTEMS ACCESSORY ELECTRODE?

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

What is the FDA product code for ASPEN SURGICAL SYSTEMS ACCESSORY ELECTRODE?

The FDA product code for ASPEN SURGICAL SYSTEMS ACCESSORY ELECTRODE is GEI.

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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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