KONICA LASER IMAGER, DRYPRO MODEL 751/752

• K Number: K013052
• Device Name: KONICA LASER IMAGER, DRYPRO MODEL 751/752
• Manufacturer: KONICA MINOLTA MEDICAL & GRAPHIC, INC.
• Date Cleared: 2002-01-16 ( 127 days)
• Product Code: LMC
• Regulation Number: 892.2040
• Type: Traditional
• Panel: Radiology
• Reference & Predicate Devices: K992586
• Predicate For: N/A

Intended Use

The Konica Laser Imager DRYPRO model 751/752 is a laser imager converts data from diagnostic equipment such as CT, MRI, DSA, and other medical devices into various intensities, scan and then print the data onto laser imaging film.

Device Description

Konica Laser Imager DRYPRO model 751/752 are laser imagers convert data from diagnostic equipment such as CT, MRI, DSA, and other medical devices into various intensities, scan and then print the data onto laser imaging film. This device consists of film supplying unit, film transferring unit, exposing unit, power supplying unit, heat-developing unit, operating unit, power supplying unit and control unit. This device is certified as a Class I laser product under 21CFR Chapter I, Subchapter J.

AI/ML Overview

The provided text is a 510(k) summary for the Konica Laser Imager DRYPRO model 751/752. This document describes a medical imaging hardcopy device that converts digital image data into physical film. It does not describe an AI medical device that generates performance metrics like accuracy, sensitivity, or specificity against ground truth. Therefore, the requested information regarding acceptance criteria, study data, sample sizes, expert qualifications, and ground truth establishment is not applicable to this document.

The document primarily focuses on:

• Identification of the company and device.
• Classification of the device (Class II per 21 CFR 892.2040).
• Description of the device's function: converting digital data from diagnostic equipment (CT, MRI, DSA) into various intensities, scanning, and printing onto laser imaging film.
• Intended Use: detailed in the device description.
• Substantial Equivalence: claiming equivalence to a predicate device (Konica Laser Imager DRYPRO model 722, K992586).
• Compliance with standards: IEC60601-1-1, IEC60601-1-2, FCC, DHHS, UL, C-UL, C-TICK.

The only "performance" aspect mentioned refers to "clinical performance" characteristics in the context of substantial equivalence to the predicate device, but no specific performance metrics or studies are detailed in the provided text. The statement "The output of the device is evaluated by additional trained personnel allowing only. sufficient review to afford identification and intervention in case of malfunction" indicates human oversight, but not a study to prove meeting acceptance criteria in the sense of AI device performance.

Summary

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510(k) Summary

as required by 807.92

1. Company Identification

JAN 1 5 2002

K013052

Konica Corporation 591-7, Kamihirose, Sayama-shi, Saitama-ken 350-1321 Japan Tel : [phone] Fax : [phone]

2. Official Correspondent

Koji Kubo (Mr.) Technical Support Department MG Imaging Equipment & Systems Development Center Medical & Graphic Company

• 3. Date of Submission
     August. 20, 2001
• 4. Device Trade name
     Konica Laser Imager, DRYPRO model 751/752
• 5. Common Name
     Laser Imager

6. Classification

Laser imager was reviewed by the Radiology Panel and are classified in Class II per 21 CFR 892.2040.

6. Description of Device

Konica Laser Imager DRYPRO model 751/752 are laser imagers convert data from diagnostic equipment such as CT, MRI, DSA, and other medical devices into various intensities, scan and then print the data onto laser imaging film.

This device consists of film supplying unit, film transferring unit, exposing unit, power supplying unit, heat-developing unit, operating unit, power supplying unit and control unit.

This device is certified as a Class I laser product under 21CFR Chapter I, Subchapter J.

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This device has no patient contacting materials and is used by trained personnel The output of the device is evaluated by additional trained personnel allowing only. sufficient review to afford identification and intervention in case of malfunction.

7. Intended Use

Konica Laser Imager DRYPRO model 751/752 convert data from diagnostic equipment such as CT, MRI, DSA, and other medical devices into various intensities, scan and then print the data onto laser imaging film.

8. Substantial Equivalence to Predicate Device

Konica Laser Imager DRYPRO model 751/752 are substantially equivalent to our Konica Laser Imager DRYPRO model 722, 510(k) number: K992586. Comparison of the principal characteristics of the two devices, which are pertinent to clinical performance is shown below.

9. Compliance with several standards

Konica Laser Imager DRYPRO model 751/752 comply with the following standards.

Safety: Electromagnetic compatibility: Applied standard: Certification granted:

IEC60601-1-1 IEC60601-1-2 FCC, DHHS UL, C-UL, C-TICK

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Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with three lines forming its body and wings. The eagle is facing right. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion around the eagle.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

JAN 1 5 2002

Konica Corporation % Mr. Shinichi Yamanaka Cosmos Corporation 319 Akeno, Obata-cho Watarai-gun, Mic-ken 519-05 Japan

Re: K013052

Trade/Device Name: Konica Laser Imager Drypro Model 751/752 Regulation Number: 21 CFR 892.2040 Regulation Name: Medical image hardcopy device Regulatory Class: II Product Code: 90 LMC Dated: November 26, 2001 Received: December 3, 2001

Dear Mr. Yamanaka:

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	[phone]
876.2xxx, 3xxx, 4xxx, 5xxx	[phone]
884.2xxx, 3xxx, 4xxx, 5xxx, 6xxx	[phone]
892.2xxx, 3xxx, 4xxx, 5xxx	[phone]
Other	[phone]

Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. 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 [phone] or [phone] 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

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510(k) Number (If known): Not known Ko / 30552

Device Name: Konica Laser Imager DRYPRO model 751/752

Indications for Use:

The Konica Laser Imager DRYPRO model 751/752 is a laser imager converts data from diagnostic equipment such as CT, MRI, DSA, and other medical devices into various intensities, scan and then print the data onto laser imaging film.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation

Prescription Use
✓

OR Over-The-Counter Use

(Optional Format 1-2-96)

Nancy C Broadon

(Division Sign-Off)
Division of Reproductive, Abdominal,
and Radiological Devices K019052
510(k) Number

Regulation Number and Section

N/A