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FDA 510(k)

MINI LAP RETRACTORS

K-Number: K093449 · 2010-02-12

ApplicantMini Lap Technologies, Inc.
Decision Date2010-02-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MINI LAP RETRACTORS 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 2010-02-12 under 510(k) number K093449. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI LAP RETRACTORS?

MINI LAP RETRACTORS is a medical device that received FDA 510(k) clearance on 2010-02-12. The listed applicant is Mini Lap Technologies, Inc.. The 510(k) number is K093449.

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

MINI LAP RETRACTORS received FDA 510(k) clearance on 2010-02-12, under 510(k) number K093449.

Who is the listed applicant for MINI LAP RETRACTORS?

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 RETRACTORS?

The FDA product code for MINI LAP RETRACTORS is GCJ.

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-TONGK083754MINI LAP ELECTROCAUTERY INSTRUMENTSK070686MINI LAP INSTRUMENTSK070352MINI LAP PEDIATRIC INSTRUMENTS WITH MEDUSA CLAMPING SYSTEM

Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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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