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FDA 510(k)

KRONNER LAPAROSCOPIC HOLDER

K-Number: K941348 · 1994-11-14

ApplicantKronner Prototypes, Inc.
Decision Date1994-11-14
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KRONNER LAPAROSCOPIC HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Kronner Prototypes, Inc.. It received FDA 510(k) clearance on 1994-11-14 under 510(k) number K941348. 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 KRONNER LAPAROSCOPIC HOLDER?

KRONNER LAPAROSCOPIC HOLDER is a medical device that received FDA 510(k) clearance on 1994-11-14. The listed applicant is Kronner Prototypes, Inc.. The 510(k) number is K941348.

When did KRONNER LAPAROSCOPIC HOLDER receive FDA 510(k) clearance?

KRONNER LAPAROSCOPIC HOLDER received FDA 510(k) clearance on 1994-11-14, under 510(k) number K941348.

Who is the listed applicant for KRONNER LAPAROSCOPIC HOLDER?

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

What is the FDA product code for KRONNER LAPAROSCOPIC HOLDER?

The FDA product code for KRONNER LAPAROSCOPIC HOLDER 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 Kronner Prototypes, 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.

K130758KRONNER SIDE-KICK UTERINE MANIPULATOR HOLDERK000663KRONNER LOW PROFILE SCOPE HOLDERK973543KRONNER LOW PROFILE SCOPE HOLDER

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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