K Number
K012136
Device Name
AVITA AGIL IT 101 INSTANT DIGITAL THERMOMETER
Manufacturer
Date Cleared
2001-09-10

(63 days)

Product Code
Regulation Number
880.2910
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
A ViTA Agil IT101 Instant Digital Thermometer is used for the intermittent measurement and monitoring of human body temperature , orally, rectally and under the arm, by consumers in the home. AviTA Agil IT101 Instant Digital Thermometer is a hand-held, non-sterile, reusable clinical thermometer intended for the determination of human temperature in either rapid mode (4-seconds orally, 6-seconds rectally and under the arm -- Predicative Temperature), or standard mode(actual determination of temperature),
Device Description
AVITA Agil IT101 Instant Digital Thermometer is a hand-held, non-sterile, reusable clinical thermometer and is designed to instantly take the body temperature orally, rectally or under the arm. With its rapidity and precisemenss, Agil IT101 gives a temperature reading in merely 4 seconds orally and 6 seconds rectally and under the arm respectively.
More Information

No
The description focuses on rapid temperature measurement using predictive algorithms, but there is no mention of AI or ML in the text provided. The performance studies reference standard compliance and bench/clinical testing, not AI/ML specific validation.

No
The device is described as an instant digital thermometer used for measuring human body temperature, which is a diagnostic function, not a therapeutic one. It does not treat or alleviate any condition.

Yes

The device is a thermometer used for measuring human body temperature, which is a diagnostic indicator for various health conditions.

No

The device description explicitly states it is a "hand-held, non-sterile, reusable clinical thermometer," indicating it is a physical hardware device, not software only.

Based on the provided information, this device 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.
  • Device Function: The ViTA Agil IT101 Instant Digital Thermometer measures human body temperature directly from the body (orally, rectally, under the arm). It does not analyze samples taken from the body.
  • Intended Use: The intended use clearly states "measurement and monitoring of human body temperature," not the analysis of biological samples.

Therefore, the device falls under the category of a clinical thermometer, which is a medical device but not an IVD.

N/A

Intended Use / Indications for Use

The AVITA Agil IT101 Instant Digital Thermometer is intended for the intermittent measurement and monitoring of human body temperature, in either Rapid mode (4-seconds orally, 6-seconds rectally and under the arm -- Predicative Temperature), or standard mode(actual determination of temperature), orally, rectally and under the arm , by consumers in the home.

AViTA Agil IT101 Instant Digital Thermometer is used for the intermittent measurement and monitoring of human body temperature , orally, rectally and under the arm, by consumers in the home.

Product codes

FLL

Device Description

AVITA Agil IT101 Instant Digital Thermometer is a hand-held, non-sterile, reusable clinical thermometer and is designed to instantly take the body temperature orally, rectally or under the arm. With its rapidity and precisemenss, Agil IT101 gives a temperature reading in merely 4 seconds orally and 6 seconds rectally and under the arm respectively.

AviTA Agil IT101 Instant Digital Thermometer is a hand-held, non-sterile, reusable clinical thermometer intended for the determination of human temperature in either rapid mode (4-seconds orally, 6-seconds rectally and under the arm -- Predicative Temperature), or standard mode(actual determination of temperature),

Mentions image processing

Not Found

Mentions AI, DNN, or ML

Not Found

Input Imaging Modality

Not Found

Anatomical Site

orally, rectally and under the arm

Indicated Patient Age Range

Not Found

Intended User / Care Setting

consumers in the home.

The device is to used and installed by people exception of handicapped persons and children.

The device is to used in the ENVIRONMENT of room temperature & normal environment condition.

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)

In terms of operating specification, Safety & EMC requirements, the device conforms to applicable standards included ASTM E1112-98, PrEN 12470-3, IEC 60601-1 and IEC 60601-1-2 requirements.

Moreover, bench testing contained in this submission and clinical testing supplied demonstrate that any differences in their technological characteristics do not raise and new questions of safety or effectiveness.

Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)

Not Found

Predicate Device(s)

Microlife IT2CA1 Digital 4-Sec. Predicative Thermometer (K990168)

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

SEP 1 0 2001

510(K) SUMMARY

K 012136

his summary of 510(k) safety and effectiveness information is being submitted in.accordance with the requirements of SMDA and 21 CFR §807.92

1.0Submitter's Name:AVITA International Corp
Address:9F, No. 78, Sec. 1, Kwang-Fu Rd., San-Chung, Taipei County, Taiwan, R.O.C.
Phone:001-886-2-85121568
Fax:001-886-2-85121347
Contact:Mr. Geo Lin, General Manager
2.0 Device Name:AVITA Agil IT101 Instant Digital Thermometer
3.0Classification:Class II
4.0 Predicate Device:Microlife IT2CA1 Digital 4-Sec. Predicative Thermometer (K990168)
5.0 Device Description:AVITA Agil IT101 Instant Digital Thermometer is a hand-held, non-sterile,
reusable clinical thermometer and is designed to instantly take the body
temperature orally, rectally or under the arm. With its rapidity and
precisemenss, Agil IT101 gives a temperature reading in merely 4 seconds orally
and 6 seconds rectally and under the arm respectively.
6.0Intended Use:The AVITA Agil IT101 Instant Digital Thermometer is intended for the
intermittent measurement and monitoring of human body temperature, in either
Rapid mode (4-seconds orally, 6-seconds rectally and under the arm --
Predicative Temperature), or standard mode(actual determination of
temperature), orally, rectally and under the arm , by consumers in the home.
7.0Performance
Summary:In terms of operating specification, Safety & EMC requirements, the device
conforms to applicable standards included ASTM E1112-98, PrEN 12470-3,
IEC 60601-1 and IEC 60601-1-2 requirements.

8. Conclusions:

:

he AVITA Agil 1T101 Instant Digital Thermometer have the same intended use and similar technological characteristics as the Microlife IT2CA1 Digital 4-Sec. Predicative Thermometer (K990168). Moreover, bench testing contained in this submission and clinical testing supplied demonstrate that any differences in their technological characteristics do not raise and new questions of safety or effectiveness. Thus, the AVTA Agil 1T101 Instant Digital Thermometer, is substantially equivalent to the predicate device.

1

Image /page/1/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo is a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the top half of the circle. Inside the circle is an abstract image of an eagle with three lines representing its wings and head. The eagle is facing to the right.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

DEC 1 8 2001

AViTA International Corporation Mr. Allen Reich Harvest Consulting Corporation 900 North Switzer Canyon Drive, #142 Flaggstaff, Arizona 86001

Re: K012136

Trade/Device Name: AViTA Agil IT101 Instant Digital Thermometer Regulation Number: 880.2910 Regulation Name: Thermometer, Electronicthermometer, Predictive Thermometer Regulatory Class: II Product Codc: FLL Dated: September 10, 2001 Received: July 9, 2001

Dear Mr. Reich:

This letter corrects our substantially equivalent letter of September 10, 2001 regarding the trade name.

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). 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.

2

Page 2 - Mr. Reich

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 531-542 of the Act); 21 CFR 1000-1050.

This letter will allow you to continue 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 and additionally Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4618 . Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at their toll free number (800) 638-2041 or at (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html.

Sincerely yours,

Timothy A. Ulatowski Director Division of Dental, Infection Control and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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Page1 of 1
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NUMBER (IF KNOWN): 510 (k)

DEVICE NAME: AViTA Agil IT101 Instant Digital Thermometer AVITA International Corp.

INDICATIONS FOR USE:

A ViTA Agil IT101 Instant Digital Thermometer is used for the intermittent measurement and monitoring of human body temperature , orally, rectally and under the arm, by consumers in the home.

AviTA Agil IT101 Instant Digital Thermometer is a hand-held, non-sterile, reusable clinical thermometer intended for the determination of human temperature in either rapid mode (4-seconds orally, 6-seconds rectally and under the arm -- Predicative Temperature), or standard mode(actual determination of temperature),

The device is to used and installed by people exception of handicapped persons and children.

The device is to used in the ENVIRONMENT of room temperature & normal environment condition.

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

Concurrence of CDRH, Office of Device Evaluation

| Prescription Use
(Per 21 CFR 801.109) | OR | Over-The-Counter
(Optional Format) | V |

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(Division Sign-Off)
Division of Dental, Infection Control,
and General Hospital Devices
510(k) NumberK012136

510(k) Number _