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FDA 510(k)

ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP

K-Number: K010007 · 2001-02-22

ApplicantTaut, Inc.
Decision Date2001-02-22
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP is the device name listed in this FDA 510(k) record. The listed applicant is Taut, Inc.. It received FDA 510(k) clearance on 2001-02-22 under 510(k) number K010007. 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 ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP?

ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP is a medical device that received FDA 510(k) clearance on 2001-02-22. The listed applicant is Taut, Inc.. The 510(k) number is K010007.

When did ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP receive FDA 510(k) clearance?

ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP received FDA 510(k) clearance on 2001-02-22, under 510(k) number K010007.

Who is the listed applicant for ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP?

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

What is the FDA product code for ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP?

The FDA product code for ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP is GCJ.

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Other records listing Taut, 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.

K023261ADAPT BALLOON OPEN ACCESS PORT, MODEL 41244K021731ADAPT OPEN ACCESS PORT, MODEL 41233K011018TAUT BALLOON CATHETER, MODEL 50640K003703TAUT-INSUFFLATION NEEDLEK992907INTRADUCERK992904MINI-PORT

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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

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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