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FDA 510(k)

MINI LAP INSTRUMENTS

K-Number: K070686 · 2007-04-05

ApplicantMini Lap Technologies, Inc.
Decision Date2007-04-05
Product CodeOCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MINI LAP 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 2007-04-05 under 510(k) number K070686. The device is classified under product code OCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI LAP INSTRUMENTS?

MINI LAP INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2007-04-05. The listed applicant is Mini Lap Technologies, Inc.. The 510(k) number is K070686.

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

MINI LAP INSTRUMENTS received FDA 510(k) clearance on 2007-04-05, under 510(k) number K070686.

Who is the listed applicant for MINI LAP 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 INSTRUMENTS?

The FDA product code for MINI LAP INSTRUMENTS is OCW.

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 RETRACTORSK083754MINI LAP ELECTROCAUTERY INSTRUMENTSK070352MINI LAP PEDIATRIC INSTRUMENTS WITH MEDUSA CLAMPING SYSTEM

Related Devices (Code: OCW)

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.

K252400Endomina EZFuse systemEndo Tools Therapeutics S.A.K243750SimpleStitch Suturing SystemEnvision EndoscopyK231240MaxTack™ Motorized Fixation DeviceCovidienK213271MedicloseTM SystemHealth Value Creation B.V., Trading AS Corporis MedicalK231553OverStitch NXT Endoscopic Suturing SystemApollo Endosurgery, Inc.K211309endomina systemEndo Tools Therapeutics S.A.

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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