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FDA 510(k)

PREGELLED DISPOS. ELECTROSURG. GROUND EL

K-Number: K810277 · 1981-03-11

ApplicantConmedcorp
Decision Date1981-03-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PREGELLED DISPOS. ELECTROSURG. GROUND EL is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1981-03-11 under 510(k) number K810277. 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 PREGELLED DISPOS. ELECTROSURG. GROUND EL?

PREGELLED DISPOS. ELECTROSURG. GROUND EL is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is Conmedcorp. The 510(k) number is K810277.

When did PREGELLED DISPOS. ELECTROSURG. GROUND EL receive FDA 510(k) clearance?

PREGELLED DISPOS. ELECTROSURG. GROUND EL received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810277.

Who is the listed applicant for PREGELLED DISPOS. ELECTROSURG. GROUND EL?

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 PREGELLED DISPOS. ELECTROSURG. GROUND EL?

The FDA product code for PREGELLED DISPOS. ELECTROSURG. GROUND EL is 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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