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FDA 510(k)

PREMIE T.D.S. ELECTROSURGICAL GROUNDING PAD

K-Number: K855084 · 1986-05-06

ApplicantConmedcorp
Decision Date1986-05-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PREMIE T.D.S. ELECTROSURGICAL GROUNDING PAD is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1986-05-06 under 510(k) number K855084. 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 PREMIE T.D.S. ELECTROSURGICAL GROUNDING PAD?

PREMIE T.D.S. ELECTROSURGICAL GROUNDING PAD is a medical device that received FDA 510(k) clearance on 1986-05-06. The listed applicant is Conmedcorp. The 510(k) number is K855084.

When did PREMIE T.D.S. ELECTROSURGICAL GROUNDING PAD receive FDA 510(k) clearance?

PREMIE T.D.S. ELECTROSURGICAL GROUNDING PAD received FDA 510(k) clearance on 1986-05-06, under 510(k) number K855084.

Who is the listed applicant for PREMIE T.D.S. ELECTROSURGICAL GROUNDING PAD?

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 PREMIE T.D.S. ELECTROSURGICAL GROUNDING PAD?

The FDA product code for PREMIE T.D.S. ELECTROSURGICAL GROUNDING PAD 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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