(20 days)
Not Found
No
The description focuses on the hardware and printing process, with no mention of AI or ML capabilities.
No
The device is described as a printer for diagnostic images, not a device used to treat or alleviate a disease or condition.
No
The device is described as a printer that produces hard copies of diagnostic images, not a device that generates or interprets diagnostic information itself.
No
The device description clearly describes a physical printer with hardware components (film input trays, print head, etc.) and a printing process, indicating it is not software-only.
Based on the provided information, the Drystar 5500 is not an In Vitro Diagnostic (IVD) device.
Here's why:
- Intended Use: The intended use clearly states that the device is a "free-standing printer used to print diagnostic images on transparent film for viewing on a standard view box." This describes a device that produces a physical output of images generated by other medical imaging devices.
- IVD Definition: IVD devices are used to examine specimens derived from the human body (like blood, urine, tissue) to provide information for diagnosis, monitoring, or screening. The Drystar 5500 does not interact with or analyze biological specimens.
- Device Description: The description focuses on the printing technology, film handling, and network capabilities. It does not mention any components or processes related to analyzing biological samples.
The Drystar 5500 is a medical device, but it falls under the category of a medical image printer, which is distinct from an IVD.
N/A
Intended Use / Indications for Use
The Drystar 5500 is a free-standing printer used to print diagnostic images on transparent film for viewing on a standard view box. It may be used in any situation in which a hard copy of an image generated by a medical imaging device is required or desirable.
Product codes
90 LMC
Device Description
The Drystar 5500 is a dry-process, B/W printer, using the direct thermal printing principle to establish continuous-tone images with medical diagnostic image quality. The printer has two film input trays and each can accept any of five sizes of film, 8x10, 10x12, 11x14, 14x14, and 14x17. Film may be loaded in full daylight. The printer is a network-only printer.
The resolution of both the Drystar 4500 and 5500 is 506 dpi. The print head in the Drystar 5500 is 14 inches wide (compared to 10 inches in the 4500), which with constant resolution means more pixels per line for the 5500.
The film for the Drystar 5500, DT2 B/C, allows for faster printing (up to 180 films per minute for the largest size film) than the TM1 B/C used with the Drystar 4500.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
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
The Drystar 5500 will be certified for electrical safety according to EN 60601-1-1 and UL-2601, and electromagnetic compatibility according to EN 60601-1-2.
Key Metrics
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 892.2040 Medical image hardcopy device.
(a)
Identification. A medical image hardcopy device is a device that produces a visible printed record of a medical image and associated identification information. Examples include multiformat cameras and laser printers.(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). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.
0
OCT 22 2002
510(k) Summary
Drvstar 5500 Dry-Process Medical Image Printer
Common/Classification Name: Medical Image Hard Copy Device 21 CFR 892.2040
Agfa Corporation 10 South Academy Street Greenville, SC 29602-9048
Contact: Jeff Jedlicka, Prepared: September 30, 2002
LEGALLY MARKETED PREDICATE DEVICES A.
On April 27, 2001, FDA cleared the Drystar 4500 printer under 510(k) number K010275. The Drystar 5500, the subject of the present Special 510(k), is a modification of the currently marketed Drystar 4500. In hardware, software, and intended use, the Drystar 5500 is substantially equivalent to the Drystar 4500.
B. DEVICE DESCRIPTION
The Drystar 5500 is a dry-process, B/W printer, using the direct thermal printing principle to establish continuous-tone images with medical diagnostic image quality. The printer has two film input trays and each can accept any of five sizes of film, 8x10, 10x12, 11x14, 14x14, and 14x17. Film may be loaded in full daylight. The printer is a network-only printer.
The resolution of both the Drystar 4500 and 5500 is 506 dpi. The print head in the Drystar 5500 is 14 inches wide (compared to 10 inches in the 4500), which with constant resolution means more pixels per line for the 5500.
The film for the Drystar 5500, DT2 B/C, allows for faster printing (up to 180 films per minute for the largest size film) than the TM1 B/C used with the Drystar 4500.
C. INTENDED USE
The Drystar 5500 is a free-standing printer used to print diagnostic images on transparent film for viewing on a standard view box. It may be
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used in any situation in which a hard copy of an image generated by a medical imaging device is required or desirable.
D. SUBSTANTIAL EQUIVALENCE SUMMARY
The Drystar 5500 is a medical device and it has the same indications for use as the legally marketed Drystar 4500. The Drystar 5500 has the same technological characteristics as the Drystar 4500, and this premarket notification has described the characteristics of the Drystar 5500 in sufficient detail to assure substantial equivalence.
E. TECHNOLOGICAL CHARACTERISTICS
The technological characteristics of the Drystar 5500 are qualitatively identical to those of the predicate device, the Drystar 4500. The Drystar 5500 and its DT2 film represent enhancements of the same basic design.
ப் TESTING
The Drystar 5500 will be certified for electrical safety according to EN 60601-1-1 and UL-2601, and electromagnetic compatibility according to EN 60601-1-2.
CONCLUSIONS G.
This pre-market submission has demonstrated Substantial Equivalence as defined and understood in Sections 513(f)(1) and 513(l)(1) of the Federal Food Drug and Cosmetic Act and various quidance documents issued by the Center for Devices and Radiological Health.
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DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/2/Picture/1 description: The image shows a circular logo with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" written around the perimeter. Inside the circle is a stylized symbol that resembles an abstract bird in flight, composed of three curved lines. The logo is black and white and appears to be a scan or photocopy due to its slightly grainy texture.
Public Health Service
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Mr. Jeffery A. Jedlicka Manager, Regulatory Affairs and Compliance AGFA Corporation 10 South Academy Street Mail Stop 100 GREENVILLE SC 29601
- Re: K023287
Trade/Device Name: Drystar 5500 Regulation Number: 21 CFR 892.2040 Regulation Name: Medical image hardcopy device Regulatory Class: II Product Code: 90 LMC Dated: September 30, 2002 Received: October 2, 2002
Dear Mr. Jedlicka:
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.
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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. Snogdon
Nancy C. Brogdon Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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STATEMENT OF INDICATIONS FOR USE
| 510(k) Number (if known): | K02 3287 | ||
|---|---|---|---|
| CALLERS SECTION SECTION CONSULTION COLLEGIONAL CONTRACTOR COLLEGIONAL COLLECTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSULTION CONSU |
Device Name: Drystar 5500
Indications For Use:
The Drystar 5500 is a free-standing printer used to print diagnostic images on transparent film for viewing on a standard view box. It may be used in any situation in which a hard copy of an image generated by a medical imaging device is required or desirable.
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use (Per 21 CFR 801.109)
OR
Over-The-Counter Use - -
lance C. Brozdon
(Division Sign-Off) Division of Reproductive, Abdominal and Radiological Devices 510(k) Number _
00003