(71 days)
None
Not Found
No
The summary does not mention AI, ML, or any related terms, and the device description is a standard intraoral camera.
No
The device is used to provide images for explanation and documentation, not for treatment or diagnosis of a disease or condition.
No
The device provides images to assist the dentist in describing procedures and results, it does not state that it is used to diagnose a condition.
No
The device description explicitly states "ZoomCam LD-10 Intraoral Camera and Accessories," indicating it includes hardware (the camera and accessories) in addition to any potential software components.
Based on the provided information, the ZoomCam LD-10 Intraoral Camera and Accessories 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. They are used to diagnose, monitor, or screen for health issues.
- ZoomCam LD-10 Function: The description clearly states the device is an "Intraoral Camera" used to "provide an image of the mouth." This is a device that captures images directly from the patient's body (the mouth) and does not involve testing samples outside the body.
- Intended Use: The intended use is to assist the dentist in describing procedures and results based on visual images of the mouth. This is a visual aid for communication and documentation, not a diagnostic test performed on a biological sample.
Therefore, the ZoomCam LD-10 falls under the category of a medical device used for imaging and visualization within the body, not an in vitro diagnostic device.
N/A
Intended Use / Indications for Use
The ZoomCam LD-10 Intraoral Camera and Accessories are indicated for use to provide a image of the mouth before and after the dental procedure, which assists the dentist in describing the dental procedure being performed as well as the results.
Product codes
EIA
Device Description
Not Found
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
mouth
Indicated Patient Age Range
Not Found
Intended User / Care Setting
dentist
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
Not Found
Key Metrics
Not Found
Predicate Device(s)
Not Found
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 872.6640 Dental operative unit and accessories.
(a)
Identification. A dental operative unit and accessories is an AC-powered device that is intended to supply power to and serve as a base for other dental devices, such as a dental handpiece, a dental operating light, an air or water syringe unit, and oral cavity evacuator, a suction operative unit, and other dental devices and accessories. The device may be attached to a dental chair.(b)
Classification. Class I (general controls). Except for dental operative unit, accessories are exempt from premarket notification procedures in subpart E of part 807 of this chapter subject to § 872.9.
0
Image /page/0/Picture/1 description: The image shows the seal of the U.S. Department of Health & Human Services. The seal is circular and contains the department's name around the perimeter. In the center of the seal is an emblem featuring a stylized caduceus, a symbol often associated with medicine and healthcare. The caduceus has a staff with two snakes entwined around it, and a pair of wings at the top.
Public Health Service
FEB 1 1 2005
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Mr. Sterling Cheng Manager Rolence Enterprise, Incorporated 18-3, Lane 231 Pu Chung Road Chungli 320, TAIWAN R.O.C
Re: K043325
Trade/Device Name: ZoomCam LD-10 Regulation Number: 872.6250 Regulation Name: Dental Chair and Accessories Regulatory Class: I Product Code: EIA Dated: November 11, 2004 Received: December 2, 2004
Dear Mr. Cheng:
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 apps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 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 such additional controls. Existing major regulations affecting (1 Nr.), it an 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.
1
Page 2 - Cheng
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. or met 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) ring reter 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 (240) 276-0115. 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 (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Chiu Lin, Ph.D.
Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
2
Indications for Use
510(k) Number (if known): K043325
Device Name: ZoomCam LD-10
Indications for Use:
The ZoomCam LD-10 Intraoral Camera and Accessories are indicated for use to provide a image of the mouth before and after the dental procedure, which assists the dentist in describing the dental procedure being performed as well as the results.
Prescription Use
AND/OR
Over-The-Counter Use
(Part 21 CFR 801 Subpart D)
(21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Susan Rupp
Page _1_of 1
Sion Sion-Off Ision of Anesthesiology, General Hospital. Intection Control, Dental Devices
Number: Kou3326