FDA 510(k)

MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUN

K-Number: K850129 · 1985-02-28

ApplicantConsolidated Medical Equipment, Inc.

Decision Date1985-02-28

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUN is the device name listed in this FDA 510(k) record. The listed applicant is Consolidated Medical Equipment, Inc.. It received FDA 510(k) clearance on 1985-02-28 under 510(k) number K850129. 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 MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUN?

MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUN is a medical device that received FDA 510(k) clearance on 1985-02-28. The listed applicant is Consolidated Medical Equipment, Inc.. The 510(k) number is K850129.

When did MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUN receive FDA 510(k) clearance?

MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUN received FDA 510(k) clearance on 1985-02-28, under 510(k) number K850129.

Who is the listed applicant for MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUN?

The FDA 510(k) record lists Consolidated Medical Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUN?

The FDA product code for MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUN 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.