(28 days)
K#992601
K#992601
No
The device description details a simple electronic thermometer using a thermistor and ASIC for calculation and display. There is no mention of AI, ML, or any complex algorithms beyond basic signal processing for temperature measurement.
No.
The device is described as an electronic clinical thermometer used to detect body temperature, which is a diagnostic function, not a therapeutic one.
Yes
The device measures body temperature, which is a vital sign used by healthcare professionals to diagnose various medical conditions.
No
The device description explicitly lists multiple hardware components including a thermistor, reference resistor, buzzer, ASIC, LCD display, and battery. It also describes physical characteristics like flexible/rigid tips and water resistance. While firmware is mentioned as an essential change, the core device is clearly a physical thermometer with integrated electronics, not a software-only device.
Based on the provided information, this device is not an In Vitro Diagnostic (IVD).
Here's why:
- IVD Definition: In Vitro Diagnostics are medical devices used to examine specimens taken from the human body, such as blood, urine, or tissue, to provide information for diagnosis, monitoring, or screening.
- Device Function: The described device is a digital thermometer that measures body temperature directly from the oral, armpit, and rectal sites. It does not analyze specimens taken from the body.
- Intended Use: The intended use is to detect body temperature, which is a direct physiological measurement, not an analysis of a biological sample.
Therefore, this device falls under the category of a general medical device for physiological measurement, not an IVD.
N/A
Intended Use / Indications for Use
The device is an electronic clinical thermometer using a thermistor to detect body temperature from the oral , armpit , and rectal in neonatal , pediatric and adult population used in the clinical and home testing .
Product codes
FLL
Device Description
The OSTI Temp-Teller High Speed Digital Thermometer(Model DT-302 DT-312 , DT-412 , DT-502) is an electronic thermometer using a thermistor as the temperature sensor . The sensor's electric signal is calculated and displayed by an ASIC (Application Specific IC)
The High Speed digital thermometer comprises: a thermistor for temperature sensing , a reference resistor for comparing the resistance of the thermistor , a buzzer for sounding effect , an ASIC and a LCD display for calculating and displaying the target temperature digitally . The system uses a 1.55 V battery for the power supply and the battery power is automatically check by the ASIC and displayed in LCD if the battery is exhausted .
The OSTI Temp-Teller High Speed Digital Thermometer (Model DT-302 , DT-312 . DT-412 . DT-502) can makes temperature taking faster , its temperature stabilize reading within 10 sec in a 37℃ water bath at ambient temperature 23+1-2°C .
DT-312 ,DT-412 is high speed digital thermometers, with flexible front tip and with power /measuring button set aside with LCD display and with water resistant function .
DT502 is high speed digital thermometers, with rigid front tip and with power /measuring button set aside with LCD display and with water resistant function .
DT302 is high speed digital thermometers, with rigid front tip and with power /measuring button on top end and with water resistant function .
The DT-302 , DT-312 , DT-412 , DT-502 is identical in functionality and performance .
The essential change include 1)Metal cap / Thermistor mechanical structure change to improve thermal transmission 2)Firm ware 3)Material 4)Shape layout and dimension .
The fundamental scientific technology of the modified device remains the same as that of the 510(k) cleared device.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
oral , armpit , and rectal
Indicated Patient Age Range
neonatal , pediatric and adult
Intended User / Care Setting
clinical and home testing
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)
Non-Clinical Tests: Compliance to applicable voluntary standards include ASTM E 1112-2000 , as well as IEC 601-1-1 and IEC 601-1-2 requirements. FDA Guidance documents include the" Deciding When to Submit a 510(k) for a Change to An Existing Device" and "The New 510(k) Paradigm: Alternate Approaches to Demonstrating Substantial Equivalence in Premarket Notifications".
Clinical Tests: Controlled human clinical studies were conducted using the OSTI Temp Teller Thermometer and predicate devices . Clinical data is presented with readings representing a conventional /currently accepted reading by oral or rectal temperature .
Conclusion: The OSTI TempTeller -High Speed Digital thermometers, model DT302 , DT312 , DT412,DT502 have the same intended use and technological characteristics as the 510(k) cleared device. Moreover, verification and validation tests contained in this submission demonstrate that the modified portions maintained its original safety and effectiveness. Those engineering changes do not: (1) affect the intended use or (2) alter the fundamental scientific of the device.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
K#992601, Vicks - Speed Read Digital Thermometer , Model V911 , V965
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 880.2910 Clinical electronic thermometer.
(a)
Identification. A clinical electronic thermometer is a device used to measure the body temperature of a patient by means of a transducer coupled with an electronic signal amplification, conditioning, and display unit. The transducer may be in a detachable probe with or without a disposable cover.(b)
Classification. Class II (performance standards). The device is exempt from the premarket notification procedures in part 807, subpart E of this chapter, subject to the limitations in § 880.9 and the following conditions for exemption:(1) Device is not a clinical thermometer with telethermographic functions;
(2) Device is not a clinical thermometer with continuous temperature measurement functions; and
(3) Appropriate analysis and testing (such as that outlined in the currently FDA-recognized editions, as appropriate, of ISO 80601-2-56, “Medical electrical equipment—Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement,” or ASTM E1965, “Standard Specification for Infrared Thermometers for Intermittent Determination of Patient Temperature,” or ASTM E1112, “Standard Specification for Electronic Thermometer for Intermittent Determination of Patient Temperature,” or ASTM E1104, “Standard Specification for Clinical Thermometer Probe Covers and Sheaths”) must validate specifications and performance of the device.
0
Image /page/0/Picture/0 description: The image shows the logo for Oriental System Technology Inc. The logo consists of a stylized eye-like symbol on the left, followed by the company name in a simple, sans-serif font. The text is arranged in two lines, with "ORIENTAL SYSTEM" on the top line and "TECHNOLOGY INC." on the bottom line.
SEP 1 0 2004 510(K) Summary
This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirement of SMDA 1990 and CFR§807.92.
The assigned 510(k) number is:
1. Submitter's Identifications:
Oriental System Technology Inc. 2F No.23, Industry E, Road 9th, Science Based Industrial Park Hsinchu, Taiwan, R.O.C
Contact:
Mr. Herman Lee General Manager
Date of Summary Preparation: August 12, 2004
2. Name of the Device:
TempTeller-High Speed Digital Thermometer , Model DT302 , DT312 , DT412,DT502
3. Information of the 510(k) Cleared Device (Predicate Device):
-
- TempTeller- Digital Thermometers, Model DT-102
510(k) Number: K#992601
- TempTeller- Digital Thermometers, Model DT-102
2.VICKS - Speed Read Digital Thermometer , Model V911 , V965
4. Device description:
The OSTI Temp-Teller High Speed Digital Thermometer(Model DT-302 DT-312 , DT-412 , DT-502) is an electronic thermometer using a thermistor as the temperature sensor . The sensor's electric signal is calculated and displayed by an ASIC (Application Specific IC)
The High Speed digital thermometer comprises: a thermistor for temperature sensing , a reference resistor for comparing the resistance of the thermistor , a buzzer for sounding effect , an ASIC and a LCD display for calculating and displaying the target temperature digitally . The system uses a 1.55 V battery
1
Image /page/1/Picture/0 description: The image shows a black and white logo. The logo consists of a circle with a spiral design inside. The spiral design has a small circle in the center. The logo is simple and modern.
ORIENTAL SYSTEM
TECHNOLOGY INC
for the power supply and the battery power is automatically check by the ASIC and displayed in LCD if the battery is exhausted .
The OSTI Temp-Teller High Speed Digital Thermometer (Model DT-302 , DT-312 . DT-412 . DT-502) can makes temperature taking faster , its temperature stabilize reading within 10 sec in a 37℃ water bath at ambient temperature 23+1-2°C .
DT-312 ,DT-412 is high speed digital thermometers, with flexible front tip and with power /measuring button set aside with LCD display and with water resistant function .
DT502 is high speed digital thermometers, with rigid front tip and with power /measuring button set aside with LCD display and with water resistant function .
DT302 is high speed digital thermometers, with rigid front tip and with power /measuring button on top end and with water resistant function .
The DT-302 , DT-312 , DT-412 , DT-502 is identical in functionality and performance .
The essential change include 1)Metal cap / Thermistor mechanical structure change to improve thermal transmission 2)Firm ware 3)Material 4)Shape layout and dimension .
The fundamental scientific technology of the modified device remains the same as that of the 510(k) cleared device.
5. Intended Use:
The device is an electronic clinical thermometer using a thermistor to detect body temperature from the oral , armpit , and rectal in neonatal , pediatric and adult population used in the clinical and home testing .
6. Comparison to Predicate Devices:
The OSTI Temp Teller High Speed Digital Thermometer , Model DT-301,DT-312 , DT-412 .DT-502are substantially equivalent to the following digital thermometers.
- TempTeller- Digital Thermometers, Model DT-102
510(k) Number: K#992601
2.VICKS -- Speed Read Digital Thermometer , Model V911 , V965
The OSTI Temp Teller High Speed Digital Thermometer , Model
DT-301,DT-312 ,DT-412 ,DT-502 have the same intended use as and are similar in design to the 510(k) cleared device.
2
Image /page/2/Picture/0 description: The image shows the logo for Oriental System Technology Inc. The logo consists of a circular symbol on the left and the company name on the right. The circular symbol is a stylized design with a swirling pattern inside a circle. The company name is written in a simple, sans-serif font.
K042202
3 of 3
7. Discussion of Non-Clinical Tests Performed for Determination of Substantial Equivalence are as follows:
Compliance to applicable voluntary standards include ASTM E 1112-2000 , as well as IEC 601-1-1 and IEC 601-1-2 requirements.
FDA Guidance documents include the" Deciding When to Submit a 510(k) for a Change to An Existing Device" and "The New 510(k) Paradigm: Alternate Approaches to Demonstrating Substantial Equivalence in Premarket Notifications".
8.Discussion of Clinical Tests Performed :
Controlled human clinical studies were conducted using the OSTI Temp Teller Thermometer and predicate devices . Clinical data is presented with readings representing a conventional /currently accepted reading by oral or rectal temperature .
9. Conclusions
The OSTI TempTeller -High Speed Digital thermometers, model DT302 , DT312 , DT412,DT502 have the same intended use and technological characteristics as the 510(k) cleared device. Moreover, verification and validation tests contained in this submission demonstrate that the modified portions maintained its original safety and effectiveness. Those engineering changes do not: (1) affect the intended use or (2) alter the fundamental scientific of the device.
3
Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo is circular and contains the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract symbol that resembles an eagle or bird in flight, composed of three curved lines.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
SEP 1 0 2004
Oriental System Technology, Incorporated C/O Ms. Susan D. Goldstein-Falk Official Correspondent MDI Consultants, Incorporated 55 Northern Boulevard, Suite 200 Great Neck. New York 11021
Re: K042202
Trade/Device Name: Temp Teller-High Speed Digital Thermometers, Models DT-302, DT-312, DT-412, DT-502 Regulation Number: 880.2910 Regulation Name: Clinical Electronic Thermometer Regulatory Class: II Product Code: FLL Dated: September 3, 2004 Received: September 7, 2004
Dear Ms. Goldstein-Falk:
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 approvisions 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 such additional controls. Existing major regulations affecting (1 wr ), it hay of cash 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.
4
Page 2 - Ms. Goldstein-Falk
Please be advised that FDA's issuance of a substantial equivalence determination does not I lease be act rood that 12 a determination that your device complies with other requirements mount that I Drivinederal statutes and regulations administered by other Federal agencies. or the receir any a 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 alle listing (2) es result in the quality systems (QS) regulation (21 CFR Part 820); and if requirences as better in 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) I mill letter 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), n you don't the Office of Compliance at (301) 594-4618. 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 maj obtain 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,
Cluts
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
5
Exhibit B
×
1 of of 1 Page
510(k) Number (if known): _
Device Name: Oriental System Technology Inc. Temp Teller High Speed Digital Thermometers, Models DT-32, DT-312, DT-412, DT502.
Indications For Use:
The device is an electronic clinical thermometer using a thermistor to The device is an olootronify on the oral, armpit and rectal in the neonatal, pediatric and adult population used in clinical and home testing.
Prescription Use (Per 21 CFR 801 Subpart D)
OR
Irene Naveau for ADW 9/10/04
Over-The Counter Use
(21 CFT 807 Subpart C)
(Division Sign-Off) (Division Sign-Off)
Division of Anesthesiology, General Hospital, Division Control, Dental Devices
510(k) Number: K042202
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)