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FDA 510(k)

KARL STORZ 3D VIDEO SYSTEM

K-Number: K001362 · 2000-07-17

ApplicantKarl Storz Imaging, Inc.
Decision Date2000-07-17
Product CodeGCI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ 3D VIDEO SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Imaging, Inc.. It received FDA 510(k) clearance on 2000-07-17 under 510(k) number K001362. The device is classified under product code GCI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ 3D VIDEO SYSTEM?

KARL STORZ 3D VIDEO SYSTEM is a medical device that received FDA 510(k) clearance on 2000-07-17. The listed applicant is Karl Storz Imaging, Inc.. The 510(k) number is K001362.

When did KARL STORZ 3D VIDEO SYSTEM receive FDA 510(k) clearance?

KARL STORZ 3D VIDEO SYSTEM received FDA 510(k) clearance on 2000-07-17, under 510(k) number K001362.

Who is the listed applicant for KARL STORZ 3D VIDEO SYSTEM?

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

What is the FDA product code for KARL STORZ 3D VIDEO SYSTEM?

The FDA product code for KARL STORZ 3D VIDEO SYSTEM is GCI.

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Other records listing Karl Storz Imaging, 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.

K003325KSI'S NEW CAMERA ARCHITECTURE (NCA) VIDEO IMAGING SYSTEMK994090KARL STORZ AUTOCLAVABLE CAMERA HEADK990154KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEMK974391KARL STORZ ENDOVISION XL ENDOSCOPIC CAMERA SYSTEMK973252KARL STORZ DIRECT COUPLED CAMERA HEADK963333OPTRONICS EPIC COLOR TELEVISION CAMERA SYSTEM (S97340)

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Related Devices (Code: GCI)

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.

K021747DEGALL LAPAROSCOPIC GALLBLADDER EXTRACTORSurgicon, Inc.K003222MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.K933515BOOTY ENDOSCOPE WARMERT-Med, Inc.K930302BIRTCHER SURE CLEAN INSTRUMENT SYSTEMBirtcher Medical Systems, Inc.K930496GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPSBirtcher Medical Systems, Inc.K922123AUTO SUTURE DISPOSABLE ENDOSCOPIC SPECIMEN POUCHUnited States Surgical, A Division of Tyco Healthc

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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