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FDA 510(k)

MINI LAP ELECTROCAUTERY INSTRUMENTS

K-Number: K083754 · 2009-11-20

ApplicantMini Lap Technologies, Inc.
Decision Date2009-11-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MINI LAP ELECTROCAUTERY INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Mini Lap Technologies, Inc.. It received FDA 510(k) clearance on 2009-11-20 under 510(k) number K083754. 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 MINI LAP ELECTROCAUTERY INSTRUMENTS?

MINI LAP ELECTROCAUTERY INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2009-11-20. The listed applicant is Mini Lap Technologies, Inc.. The 510(k) number is K083754.

When did MINI LAP ELECTROCAUTERY INSTRUMENTS receive FDA 510(k) clearance?

MINI LAP ELECTROCAUTERY INSTRUMENTS received FDA 510(k) clearance on 2009-11-20, under 510(k) number K083754.

Who is the listed applicant for MINI LAP ELECTROCAUTERY INSTRUMENTS?

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

What is the FDA product code for MINI LAP ELECTROCAUTERY INSTRUMENTS?

The FDA product code for MINI LAP ELECTROCAUTERY INSTRUMENTS is GEI.

Related Clinical Trials

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.

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Other records listing Mini Lap Technologies, Inc. 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.

K101101MINI-TONGK093449MINI LAP RETRACTORSK070686MINI LAP INSTRUMENTSK070352MINI LAP PEDIATRIC INSTRUMENTS WITH MEDUSA CLAMPING SYSTEM

Related Devices (Code: 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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