(15 days)
Not Found
No
The summary describes standard digital imaging processing features (Last Image Hold, Digital Subtraction, image acquisition, review, and sending) and hardware/software for image processing. There is no mention of AI, ML, deep learning, training data, or performance metrics typically associated with AI/ML algorithms.
No
The device is intended to assist physicians for diagnostic purposes and is required for interventional procedures by providing digital imaging functionality (e.g., Last Image Hold, Digital Subtraction, viewing, reviewing, and processing digital images). It is an option to X-ray systems for RF diagnostic and interventional vascular procedures. This indicates a diagnostic and image processing purpose, not a therapeutic one where the device would treat or manage a disease or condition.
Yes
The "Intended Use / Indications for Use" section explicitly states that the device is "intended to assist physicians for diagnostic purposes".
No
The device description explicitly states that the Digital Imaging option comprises an "image processing subsystem that consists of digital imaging hardware & software." This indicates the presence of hardware components in addition to the software.
Based on the provided text, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In vitro diagnostics are tests performed on samples taken from the human body, such as blood, urine, or tissue, to detect diseases, conditions, or infections.
- Device Function: The description clearly states that this device is a "Digital Imaging option" for an X-ray system (RF-Diagnost Eleva and MultiDiagnost Eleva). It processes and displays digital images acquired from a CCD camera, which is part of the X-ray system.
- Input: The input is "digital images from the CCD camera," not biological samples.
- Intended Use: The intended use is to "assist physicians for diagnostic purposes" by providing digital imaging functionality for X-ray procedures. This is related to medical imaging, not in vitro testing.
The device is a component of a medical imaging system used for diagnostic and interventional procedures, which falls under the category of medical devices, but not specifically in vitro diagnostics.
N/A
Intended Use / Indications for Use
The Digital Imaging option release 1 is intended to assist physicians for diagnostic purposes and is required for interventional procedures, providing digital functionality as Last Image Hold, Digital Subtraction and contains a user interface for viewing, reviewing and processing digital images. The Digital Imaging option release 1 includes the following features, such as :
-
- Providing Digital Acquisition or Fluoroscopy for Philips RF systems.
-
- Diagnostic and/or Interventional applications.
-
- Live subtracted acquisition and fluoroscopy for vascular applications.
-
- Single or multiple images can be acquired and reviewed.
-
- Sending digital images to printer, external workstations for post processing and reconstructions, PACS.
Product codes
90-IZI, 90 LLZ
Device Description
The Digital Imaging is an option to the RF-Diagnost Eleva system family, comprising of an image processing subsystem that consists of digital imaging hardware & software. It receives digital images from the CCD camera in the RF-Diagnost Eleva system and is intended to be placed in the examination room.
The MultiDiagnost Eleva system is an X-ray systems for RF diagnostic and interventional vascular procedures. The Philips MultiDiagnost features a remote controlled C-arm stand that can be configured with a 38 cm Image Intensifier.
The Digital Imaging for the MultiDiagnost Eleva system allows the user to acquire digital images to be postprocessed, and reviewed on the examination monitor. The progressive display black and white output signal is suitable for CRT or LCD monitor types. The (RIS) patient data provided by the system controller can be merged with the images.
Mentions image processing
The Digital Imaging is an option to the RF-Diagnost Eleva system family, comprising of an image processing subsystem that consists of digital imaging hardware & software.
The Digital Imaging for the MultiDiagnost Eleva system allows the user to acquire digital images to be postprocessed, and reviewed on the examination monitor.
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
X-ray
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
physicians / examination room
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
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).
Not Found
§ 892.2050 Medical image management and processing system.
(a)
Identification. A medical image management and processing system is a device that provides one or more capabilities relating to the review and digital processing of medical images for the purposes of interpretation by a trained practitioner of disease detection, diagnosis, or patient management. The software components may provide advanced or complex image processing functions for image manipulation, enhancement, or quantification that are intended for use in the interpretation and analysis of medical images. Advanced image manipulation functions may include image segmentation, multimodality image registration, or 3D visualization. Complex quantitative functions may include semi-automated measurements or time-series measurements.(b)
Classification. Class II (special controls; voluntary standards—Digital Imaging and Communications in Medicine (DICOM) Std., Joint Photographic Experts Group (JPEG) Std., Society of Motion Picture and Television Engineers (SMPTE) Test Pattern).
0
OCT 3 0 2002
Image /page/0/Picture/1 description: The image shows the Philips logo, which is a shield shape with the word "PHILIPS" at the top. Inside the shield, there is a globe-like symbol with wavy lines across the middle. The globe has a cross-like design on either side of the wavy lines. The logo is in black and white.
Philips Medical Systems
KO23440
510(k) SUMMARY
The following information is being submitted in accordance with the requirements of 21 CFR 807.92.
| Company Name:
Address: | Philips Medical Systems North America Company
22100 Bothell Everett Highway
P.O.Box 3003
Bothell, WA 98041-3003, USA |
|-----------------------------------|-------------------------------------------------------------------------------------------------------------------------------|
| Registration No.: | 1217116 |
| Contact Person:
Telephone No.: | Lynn Harmer
(425) 487-7312 |
| Date Prepared: | September 30, 2002 |
| Device (Trade) Name: | Philips Digital Imaging option release 1 |
| Classification Name: | Cine or spot fluorographic x-ray camera, 21 CFR 892.1650
Class II (90-IZI) |
Predicate Device:
The Philips Digital Imaging option release 1 is substantially equivalent to the Philips DSI, release 3.2, manufactured by Philips Medical Systems. The Philips DSI, release 3.2 received a 510(k) substantially equivalent determination in K920793 on July 17. 1992.
Device description:
The Digital Imaging is an option to the RF-Diagnost Eleva system family, comprising of an image processing subsystem that consists of digital imaging hardware & software. It receives digital images from the CCD camera in the RF-Diagnost Eleva system and is intended to be placed in the examination room.
The MultiDiagnost Eleva system is an X-ray systems for RF diagnostic and interventional vascular procedures. The Philips MultiDiagnost features a remote controlled C-arm stand that can be configured with a 38 cm Image Intensifier.
The Digital Imaging for the MultiDiagnost Eleva system allows the user to acquire digital images to be postprocessed, and reviewed on the examination monitor. The progressive display black and white output signal is suitable for CRT or LCD monitor types. The (RIS) patient data provided by the system controller can be merged with the images.
1
Image /page/1/Picture/1 description: The image shows the seal of the Department of Health & Human Services. The seal features a stylized caduceus, a symbol often associated with medicine and healthcare, with three diagonal lines representing the branches of government. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES" is arranged in a circular pattern around the caduceus. The seal is black and white and appears to be a scanned image.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
OCT 3 0 2002
Philips Medical Systems % Michael Kwan, Ph.D. Office Coordinator, 510(k) Review Program Medical Device Services Underwriters Laboratories, Inc. 1655 Scott Blvd. SANTA CLARA CA 95050-4169
Re: K023440 Trade/Device Name: PHILIPS Digital Imaging Option Release 1 Regulation Number: 21 CFR 892.2050 Regulation Name: Picture archiving and communications system Regulatory Class: II Product Code: 90 LLZ
Dated: October 10, 2002 Received: October 15, 2002
Dear Dr. Kwan:
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.
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 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); 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.
2
This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at one of the following numbers, based on the regulation number at the top of this letter:
| 8xx.1xxx | (301) 594-4591 |
|---|---|
| 876.2xxx, 3xxx, 4xxx, 5xxx | (301) 594-4616 |
| 884.2xxx, 3xxx, 4xxx, 5xxx, 6xxx | (301) 594-4616 |
| 892.2xxx, 3xxx, 4xxx, 5xxx | (301) 594-4654 |
| Other | (301) 594-4692 |
Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html.
Sincerely yours,
Nancy C. Brogdon
Nancy C. Brogdon Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
3
510(k) Number (if known): Unknown K C2344 O
023440
Device Name: Philips Digital Imaging option release 1
Indications for Use:
The Digital Imaging option release 1 is intended to assist physicians for diagnostic purposes and is required for interventional procedures, providing digital functionality as Last Image Hold, Digital Subtraction and contains a user interface for viewing, reviewing and processing digital images. The Digital Imaging option release 1 includes the following features, such as :
-
- Providing Digital Acquisition or Fluoroscopy for Philips RF systems.
-
- Diagnostic and/or Interventional applications.
-
- Live subtracted acquisition and fluoroscopy for vascular applications.
-
- Single or multiple images can be acquired and reviewed.
-
- Sending digital images to printer, external workstations for post processing and reconstructions, PACS.
Concurrence of Center for Devices and Radiological Health, Office of Device Evaluation
Prescription Use ✓
David A. Segmon
Division Sian-O Division of Reproductive. A and Radiological Devices 510(k) Number