(185 days)
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Not Found
No
The summary describes a standard video imaging system for endoscopy and does not mention any AI or ML capabilities, image processing beyond basic video display, or performance studies related to algorithmic analysis.
No
The device is described as a video imaging system for endoscopes, used to display endoscopic images. It does not perform any therapeutic function.
No.
Explanation: The device is described as a video imaging system for displaying endoscopic images, which aids in visualization during procedures but does not inherently diagnose conditions. Its intended use is to display images, not to perform analysis for diagnostic purposes.
No
The device description explicitly states it is a "color, television camera system" and mentions a "camera head," indicating it includes hardware components.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states that the system is a "color, television camera system intended for use with rigid or flexible endoscopes" to display endoscopic images on a monitor. This describes a system used for visualization during medical procedures, not for testing samples taken from the body (in vitro).
- Device Description: The description reinforces that it's a "color, television camera system intended for use with rigid or flexible endoscopes."
- Lack of IVD Characteristics: There is no mention of analyzing biological samples, detecting analytes, or providing diagnostic information based on laboratory tests.
IVD devices are used to examine specimens (like blood, urine, tissue) outside of the body to provide information for diagnosis, monitoring, or screening. This device is used for direct visualization within the body during a procedure.
N/A
Intended Use / Indications for Use
The Karl Storz Imaging (KSI) New Camera Architecture (NCA) Video Imaging System is a color, television camera system intended for general endoscopic use. This camera system is intended to be used with rigid or flexible endoscopes, such as sinoscopes, colonoscopes, enteroscopes, bronchoscopes, gastroscopes, cystoscopes, hysteroscopes, laparoscopes, choledocho scopes, and arthroscopes. The camera head is coupled to the endoscopic image and the image can be displayed on any standard operating room video monitor. All standard endoscopic light sources may be used with New Camera Architecture (NCA) System. This camera heads will be available in NTSC and PAL configurations.
Product codes
FET, GCJ
Device Description
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Mentions image processing
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Mentions AI, DNN, or ML
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Input Imaging Modality
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Anatomical Site
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Indicated Patient Age Range
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Intended User / Care Setting
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Description of the training set, sample size, data source, and annotation protocol
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Description of the test set, sample size, data source, and annotation protocol
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Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
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Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
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Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
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Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
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Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
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§ 876.1500 Endoscope and accessories.
(a)
Identification. An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.(b)
Classification —(1)Class II (special controls). The device, when it is an endoscope disinfectant basin, which consists solely of a container that holds disinfectant and endoscopes and accessories; an endoscopic magnetic retriever intended for single use; sterile scissors for cystoscope intended for single use; a disposable, non-powered endoscopic grasping/cutting instrument intended for single use; a diagnostic incandescent light source; a fiberoptic photographic light source; a routine fiberoptic light source; an endoscopic sponge carrier; a xenon arc endoscope light source; an endoscope transformer; an LED light source; or a gastroenterology-urology endoscopic guidewire, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.(2) Class I for the photographic accessories for endoscope, miscellaneous bulb adapter for endoscope, binocular attachment for endoscope, eyepiece attachment for prescription lens, teaching attachment, inflation bulb, measuring device for panendoscope, photographic equipment for physiologic function monitor, special lens instrument for endoscope, smoke removal tube, rechargeable battery box, pocket battery box, bite block for endoscope, and cleaning brush for endoscope. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807of this chapter, subject to the limitations in § 876.9.
0
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
Karl Storz Imaging, Inc. Mr. Terry Fernandez Director, Regulatory and Standards Compliance 175 Cremona Drive Goleta, CA 93117
JUL 2 7 2015
Re: K003325
Trade/Device Name: KSI's New Camera Architecture (NCA) Video Imaging System Regulation Number: 21 CFR 876.1500 Regulation Name: Endoscope and accessories Regulatory Class: II Product Code: FET, GCJ Dated (Date on orig SE ltr): January 31, 2001 Received (Date on orig SE ltr): February 1, 2001
Dear Mr. Fernandez,
This letter corrects our substantially equivalent letter of April 27, 2001.
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be
1
Page 2 -
found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638 2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours.
Benjamin R. Fisher -S
Beniamin R. Fisher, Ph.D. Director Division of Reproductive, Gastro-Renal, and Urological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
2
of 1 Page 1
KOO3325 510(k) Number (if known):
Device Name: KSI NEW CAMERA ARCHITECTURE (NCA) VIDEO IMAGAING SYSTEM
Indication for Use:
The Karl Storz Imaging (KSI) New Camera Architecture (NCA) Video Imaging System is a The Kall Storz maging (for) Now Samera with rigid or flexible endoscopes, such color, television camora oyotem inmoitoscopes, bronchoscopes, gastroscopes, as sinoscopes, colonooopoo, eighteiters copes, hysteroscopes and arthroscopes. The laparoscopes, choledoonoooopes, are corre. Any compatible NCA camera head may be us camera nead is would to the endoscopic image can be displayed image can be displayed on any standard operating room video monitor.
All standard endoscopic light sources may be used with New Camera Architecture (NGA) All Standard endosopio igns course thip camera heads will be available in NTSC and PAL configurations.
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED.)
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off)
510(k) Number _
Prescription Use (Per 21 CFR 801.109) Over-The-Counter Use_
Gavin C. Sygm
(Division Sign-Off)
(Optional Format 1-2-96)
Division of Reproductive, Abdominal, ENT, and Radiological Device 510(k) Number
OR
0000018