← Product Code [LMA](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LMA) · K063424 # FILM DIGITZER, MODEL 2908 MAMMO PRO (K063424) _Array Corp. · LMA · Dec 21, 2006 · Radiology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LMA/K063424 ## Device Facts - **Applicant:** Array Corp. - **Product Code:** [LMA](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LMA.md) - **Decision Date:** Dec 21, 2006 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 892.2030 - **Device Class:** Class 2 - **Review Panel:** Radiology ## Intended Use Model 2908 Mammo pro is intended for covering analog Medical x-ray films to digital images. The device is indicated for the digitization of mammography Imaged for review and analysis, but not as the sole basis for screening or diagnosis. The device is indicated for the digitization of mammography images for storage and display not for primary image diagnosis. ## Device Story Film Digitizer Model 2908 Mammo Pro converts analog medical x-ray films into digital images. Device operates by scanning physical film to produce digital output for storage, display, and review. Used in clinical settings by healthcare professionals. Output assists in image management and review workflows; not intended for primary diagnostic interpretation or as the sole basis for screening. Benefits include transition of analog mammography archives to digital formats for improved accessibility and storage. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Medical image digitizer; converts analog x-ray film to digital format. Operates as a peripheral device for image storage and display systems. Class II device under 21 CFR 892.2030. ## Regulatory Identification A medical image digitizer is a device intended to convert an analog medical image into a digital format. Examples include systems employing video frame grabbers, and scanners which use lasers or charge-coupled devices. ## Special Controls *Classification.* Class II (special controls; voluntary standards—Digital Imaging and Communications in Medicine (DICOM) Std., Joint Photographic Experts Group (JPEG) Std.). 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. ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ Food and Drug Administration 9200 Corporate Blvd. Rockville MD 20850 Mr. Takashi Inami Manager ARRAY Corp. 3-42-10 Yoyogi Sibuya-ku, Tokyo, 151-0053 JAPAN DEC 2 1 2006 Re: K063424 Trade/Device Name: Film Digitizer, Model 2908 Mammo Pro Regulation Number: 21 CFR 892.2030 Regulation Name: Medical image digitizer Regulatory Class: II Product Code: LMA Dated: November 6, 2006 Received: November 13, 2006 Dear Mr. Inami: 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 (Premarket Approval), it may be subject to such 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. Image /page/0/Picture/9 description: The image is a circular logo with the text "1906-2006" at the top. Below that is the text "FDA Centennial" in a stylized font. There are three stars at the bottom of the logo. The logo appears to be a commemorative emblem for the 100th anniversary of the Food and Drug Administration. Protecting and Promoting Public Health {1}------------------------------------------------ Page 2 - 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. This letter will allow you to begin marketing your device as described in your Section 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: | 21 CFR 876.xxx | (Gastroenterology/Renal/Urology) | 240-276-0115 | |----------------|----------------------------------|--------------| | 21 CFR 884.xxx | (Obstetrics/Gynecology) | 240-276-0115 | | 21 CFR 894.xxx | (Radiology) | 240-276-0120 | | Other | | 240-276-0100 | Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). 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 (240) 276-3150 or at its Internet address http://www.fda.gov/cdrl/industry/support/index.html. Sincerely yours, Nancy Cbrogdon Nancy C. Brogdon Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## Indications for Use 510(k) Number (if known): K063424 Film Digitizer, Model 2908 Mammo Pro Device Name : Indications For Use: Model 2908 Mammo pro is intended for covering analog Medical x-ray films to digital images. The device is indicated for the digitization of mammography Imaged for review and analysis, but not as the sole basis for screening or diagnosis. The device is indicated for the digitization of mammography images for storage and display not for primary image diagnosis. Prescription Use (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) David A. Seggern (Division Sign-Off) Division of Reproductive, Abdor and Radiological Devices 510(k) Numb --- **Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LMA/K063424](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/LMA/K063424) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com