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FDA 510(k)

HABIB LAPAROSCOPIC HEXABLATE

K-Number: K073687 · 2008-01-09

ApplicantEmcision , Ltd.
Decision Date2008-01-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HABIB LAPAROSCOPIC HEXABLATE is the device name listed in this FDA 510(k) record. The listed applicant is Emcision , Ltd.. It received FDA 510(k) clearance on 2008-01-09 under 510(k) number K073687. 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 HABIB LAPAROSCOPIC HEXABLATE?

HABIB LAPAROSCOPIC HEXABLATE is a medical device that received FDA 510(k) clearance on 2008-01-09. The listed applicant is Emcision , Ltd.. The 510(k) number is K073687.

When did HABIB LAPAROSCOPIC HEXABLATE receive FDA 510(k) clearance?

HABIB LAPAROSCOPIC HEXABLATE received FDA 510(k) clearance on 2008-01-09, under 510(k) number K073687.

Who is the listed applicant for HABIB LAPAROSCOPIC HEXABLATE?

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

What is the FDA product code for HABIB LAPAROSCOPIC HEXABLATE?

The FDA product code for HABIB LAPAROSCOPIC HEXABLATE is GEI.

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Other records listing Emcision , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K180165Habib EndoHPBK161305Habib EUS RFAK083292HABIB ENDOHPBK080717HABIB HEXABLATE 10K072383HABIB ENDOBLATEK072126HABIB VESEAL

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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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