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FDA 510(k)

LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE

K-Number: K912637 · 1991-10-04

ApplicantDexide, Inc.
Decision Date1991-10-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1991-10-04 under 510(k) number K912637. 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 LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE?

LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE is a medical device that received FDA 510(k) clearance on 1991-10-04. The listed applicant is Dexide, Inc.. The 510(k) number is K912637.

When did LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE receive FDA 510(k) clearance?

LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE received FDA 510(k) clearance on 1991-10-04, under 510(k) number K912637.

Who is the listed applicant for LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE?

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

What is the FDA product code for LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE?

The FDA product code for LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE is GEI.

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Other records listing Dexide, Inc. as applicant

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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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