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FDA 510(k)

EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU

K-Number: K844780 · 1985-05-21

ApplicantPoly- Med, Inc.
Decision Date1985-05-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU is the device name listed in this FDA 510(k) record. The listed applicant is Poly- Med, Inc.. It received FDA 510(k) clearance on 1985-05-21 under 510(k) number K844780. 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 EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU?

EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU is a medical device that received FDA 510(k) clearance on 1985-05-21. The listed applicant is Poly- Med, Inc.. The 510(k) number is K844780.

When did EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU receive FDA 510(k) clearance?

EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU received FDA 510(k) clearance on 1985-05-21, under 510(k) number K844780.

Who is the listed applicant for EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU?

The FDA 510(k) record lists Poly- Med, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU?

The FDA product code for EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU is GEI.

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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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