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FDA 510(k)

ASCENTEC MEDICZAL SYSTEMS LAPAROSCOPIC ELECTRODE

K-Number: K914252 · 1991-12-13

ApplicantAscentec Medical Systems
Decision Date1991-12-13
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ASCENTEC MEDICZAL SYSTEMS LAPAROSCOPIC ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Ascentec Medical Systems. It received FDA 510(k) clearance on 1991-12-13 under 510(k) number K914252. 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 ASCENTEC MEDICZAL SYSTEMS LAPAROSCOPIC ELECTRODE?

ASCENTEC MEDICZAL SYSTEMS LAPAROSCOPIC ELECTRODE is a medical device that received FDA 510(k) clearance on 1991-12-13. The listed applicant is Ascentec Medical Systems. The 510(k) number is K914252.

When did ASCENTEC MEDICZAL SYSTEMS LAPAROSCOPIC ELECTRODE receive FDA 510(k) clearance?

ASCENTEC MEDICZAL SYSTEMS LAPAROSCOPIC ELECTRODE received FDA 510(k) clearance on 1991-12-13, under 510(k) number K914252.

Who is the listed applicant for ASCENTEC MEDICZAL SYSTEMS LAPAROSCOPIC ELECTRODE?

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

What is the FDA product code for ASCENTEC MEDICZAL SYSTEMS LAPAROSCOPIC ELECTRODE?

The FDA product code for ASCENTEC MEDICZAL SYSTEMS LAPAROSCOPIC ELECTRODE 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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