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FDA 510(k)

CONMED STEALTH NON-STICK ACCESSORY ELECTRODE, MODEL 138XXX

K-Number: K991855 · 1999-06-15

ApplicantConmedcorp
Decision Date1999-06-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONMED STEALTH NON-STICK ACCESSORY ELECTRODE, MODEL 138XXX is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1999-06-15 under 510(k) number K991855. 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 CONMED STEALTH NON-STICK ACCESSORY ELECTRODE, MODEL 138XXX?

CONMED STEALTH NON-STICK ACCESSORY ELECTRODE, MODEL 138XXX is a medical device that received FDA 510(k) clearance on 1999-06-15. The listed applicant is Conmedcorp. The 510(k) number is K991855.

When did CONMED STEALTH NON-STICK ACCESSORY ELECTRODE, MODEL 138XXX receive FDA 510(k) clearance?

CONMED STEALTH NON-STICK ACCESSORY ELECTRODE, MODEL 138XXX received FDA 510(k) clearance on 1999-06-15, under 510(k) number K991855.

Who is the listed applicant for CONMED STEALTH NON-STICK ACCESSORY ELECTRODE, MODEL 138XXX?

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 CONMED STEALTH NON-STICK ACCESSORY ELECTRODE, MODEL 138XXX?

The FDA product code for CONMED STEALTH NON-STICK ACCESSORY ELECTRODE, MODEL 138XXX 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 Conmedcorp 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.

View all 92 devices →

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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