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FDA 510(k)

ELECTROSURGICAL LAPAROSCOPIC INSTRUMENT

K-Number: K942915 · 1994-07-08

ApplicantMorgan Medical Co.
Decision Date1994-07-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL LAPAROSCOPIC INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Morgan Medical Co.. It received FDA 510(k) clearance on 1994-07-08 under 510(k) number K942915. 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 ELECTROSURGICAL LAPAROSCOPIC INSTRUMENT?

ELECTROSURGICAL LAPAROSCOPIC INSTRUMENT is a medical device that received FDA 510(k) clearance on 1994-07-08. The listed applicant is Morgan Medical Co.. The 510(k) number is K942915.

When did ELECTROSURGICAL LAPAROSCOPIC INSTRUMENT receive FDA 510(k) clearance?

ELECTROSURGICAL LAPAROSCOPIC INSTRUMENT received FDA 510(k) clearance on 1994-07-08, under 510(k) number K942915.

Who is the listed applicant for ELECTROSURGICAL LAPAROSCOPIC INSTRUMENT?

The FDA 510(k) record lists Morgan Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROSURGICAL LAPAROSCOPIC INSTRUMENT?

The FDA product code for ELECTROSURGICAL LAPAROSCOPIC INSTRUMENT 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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