(120 days)
Powder Free Latex Examination Gloves, Non Sterile (contains 50 micrograms/dm² or less of total water extractable protein) is a disposable device and made of Natural Rubber Latex intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner.
Powder Free Latex Examination Gloves, Non Sterile (contains The 50 micrograms/dm² or less of total water extractable protein) is Class I Device. These gloves are made of natural rubber latex. The gloves can be used either right or left hand (ambidextrous), Disposable, Single Use and Non Sterile. The Specification of this device meets the requirements of ASTM Standard D 3578 - 05 and FDA 1000ml Water Leak Test.
Here's a breakdown of the acceptance criteria and the study information based on the provided document:
1. Table of Acceptance Criteria and Reported Device Performance
| Characteristics | Standards | Acceptance Criteria (Implied) | Reported Device Performance |
|---|---|---|---|
| Dimensions | D 3578 – 05 | Conformance to D 3578 – 05 | Meets |
| Physical Properties | D 3578 – 05 | Conformance to D 3578 – 05 | Meets |
| Freedom from Pinholes | FDA 21 CFR 800.20 | Conformance to FDA 21 CFR 800.20 | Meets |
| Powder Residue | D 3578 – 05, D 6124 – 06 | < 2 mg/gloves | < 2 mg/gloves |
| Water Soluble Protein Content | D 3578 – 05, D 5712 – 10 | < 50µg/dm² | < 50µg/dm² |
| Biocompatibility (Primary Skin Irritation) | 16 CFR Ch.ll 1500, 4.1 (Rabbits) | Passes (No primary skin irritation) | Passes (No primary skin irritation) |
| Biocompatibility (Dermal Sensitization) | ASTM F720-81 | Passes (No contact sensitizer) | Passes (No contact sensitizer) |
| Water Leak Test | FDA 1000ml Water Leak Test | Conformance to FDA 1000ml Water Leak Test | Meets |
2. Sample Size and Data Provenance (for test set/performance data)
The document does not explicitly state the sample sizes used for each specific test. However, it implies that tests were conducted on the "Powder Free Latex Examination Gloves" to ensure they meet the defined standards.
- Data Provenance: The document does not specify the country of origin for the data itself, but the manufacturer is PT. INTAN HEVEA INDUSTRY, located in Indonesia. The studies appear to be retrospective in the sense that they are reporting on tests conducted on already produced gloves to demonstrate compliance with established standards.
3. Number of Experts and Qualifications (for establishing ground truth)
- This information is not applicable to this type of device and study. The "ground truth" here is objective measurement against established ASTM and FDA standards for physical, chemical, and biological properties, not expert interpretation of medical images or clinical outcomes.
4. Adjudication Method (for test set)
- This information is not applicable. The tests are objective measurements against defined criteria, not subjective assessments requiring adjudication.
5. Multi Reader Multi Case (MRMC) Comparative Effectiveness Study
- No, an MRMC comparative effectiveness study was not done. This type of study is relevant for diagnostic devices where human readers interpret results, often with and without AI assistance, to assess the AI's impact on diagnostic accuracy or efficiency. This document describes an examination glove, which is not a diagnostic device.
6. Standalone Performance Study
- Yes, in a broad sense, a standalone performance assessment was done. The document outlines a series of non-clinical tests conducted on the examination gloves themselves to demonstrate their inherent physical, chemical, and biological properties without human intervention or interpretation (beyond conducting the tests). The "Performance" column in the table effectively reports the standalone performance of the device against predefined standards.
7. Type of Ground Truth Used
- The ground truth used is based on objective measurements and adherence to established industry and regulatory standards. These standards define acceptable ranges or outcomes for physical properties (dimensions, physical strength), chemical properties (powder residue, protein content), and biological properties (biocompatibility). For example, a glove "Meets" the freedom from pinholes test if it passes the FDA 21 CFR 800.20 methodology.
8. Sample Size for the Training Set
- This information is not applicable. This device is a physical product (examination glove), not an AI/ML algorithm that requires a training set.
9. How the Ground Truth for the Training Set Was Established
- This information is not applicable since there is no training set for this type of device.
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NOV - 4 2011
PT. INTAN HEVEA INDUSTRY
Jalan Pulau trian No. 13 Kawasan Industri Medan I Jalan Yos Sudarso Km 10.5. Medan 20371. INDONESIA
| Tel | +62-61-6850169 |
|---|---|
| +62-61-6856335 | |
| Fax | +62-61-6850168 |
| +62-61-6856335 | |
| intanhevea@yahoo.com |
510k Summary
1.0
| Submitter : | |
|---|---|
| Name | : PT. INTAN HEVEA INDUSTRY |
| Address | : Jalan Pulau Irian No.13 Kawasan Industri Medan I Jalan Yos Sudarso Km 10.5 Medan 20371, INDONESIA |
| Phone No. | : +62-61-6850169, 6856335 |
| Fax No. | : +62-61-6850168, 6856335 |
Date of Summary Prepared : September 19, 2011
2.0 Contact Person :
| Name | : Darwin Tandjo |
|---|---|
| Phone No. | : +62-61-6850169, 6856335 |
| Fax No. | : +62-61-6850168, 6856335 |
3.0 Name of the Device :
| Trade Name | : SKIN GUARD and Multiple or Customer's Trade Name |
|---|---|
| Device Name | : Powder Free Latex Examination Gloves, Non Sterile(contains 50 micrograms/ dm² or less of total waterextractable protein). |
| Common Name | : Examination Gloves |
| Classification Name | : Patient Examination Gloves (Class I) |
4.0 Identification of The Legally Marketed Device (Predicate Device) which Substantially Equivalent:
The Powder Free Latex Examination Gloves, Non Sterile (contains 50 micrograms/dm2 or less of total water extractable protein) are substantially equivalent with Latex Patient Examination Gloves, Powdered, Non-Sterile submitted and cleared under 510(k) number K894480. The different in this submission is the product Powder Free, Non Sterile with labeling claim contains 50 micrograms/dm² or less of total water extractable protein with no change in product design.
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Image /page/1/Picture/0 description: The image shows a black and white drawing of a diamond. The diamond has a geometric shape with several facets. A vertical line extends from the bottom point of the diamond downwards. The drawing is simple and lacks shading or color.
PT. INTAN HEVEA INDUSTRY
Jalan Pulau Irian No. 13 Kawasan Industri Medan I Jalan Yos Sudarso Km 10.5. Medan 20371. INDONESIA.
Tel +62-61-6850169 +62-61-6856335 Fax 62-61-6850168 +62-61-6856335 Email intanhevea@yahoo.com
5.0 Description and Specification of The Device :
Powder Free Latex Examination Gloves, Non Sterile (contains The 50 micrograms/dm² or less of total water extractable protein) is Class I Device. These gloves are made of natural rubber latex. The gloves can be used either right or left hand (ambidextrous), Disposable, Single Use and Non Sterile. The Specification of this device meets the requirements of ASTM Standard D 3578 - 05 and FDA 1000ml Water Leak Test.
6.0 Intended Use of the Device :
The Powder Free Latex Examination Gloves (contains 50 micrograms/dm² or less of total water extractable protein) is a disposable device intended for medical purpose that is worn on the examiners hand and finger to prevent contamination between patient and examiner.
7.0 Summary of The Technological Characteristics of The Device :
The Powder Free Latex Examination Gloves, (contains 50 micrograms/dm² or less of total water extractable protein) technological characteristics are summarized in the following information compared with ASTM or equivalent standards ;
| Characteristics | Standards | Performance |
|---|---|---|
| Dimensions | D 3578 – 05 | Meets |
| Physical Properties | D 3578 – 05 | Meets |
| Freedom from Pinholes | FDA 21 CFR 800.20 | Meets |
| Powder Residue | D 3578 – 05D 6124 – 06 | <2 mg/gloves |
| Water Soluble ProteinContent | D 3578 – 05D 5712 – 10 | < 50µg/dm² |
| Biocompatibility | 16 CFR Ch.ll 1500, 4.1Primary Skin Irritation inRabbitsASTM F720-81 DermalSensitization | Passes (No primary skinirritation)Passes (No contactsensitizer) |
8.0 Substantial Equivalent Based on Assessment of Non-Clinical Performance Data : The performance test data of the non clinical tests that support a determination of substantial equivalent is the same as mentioned immediately above.
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Image /page/2/Picture/0 description: The image is a black and white drawing of a diamond shape. The diamond is divided into five sections, with the middle section being the largest. The two sections on either side of the middle section are smaller, and the two sections on the outside are the smallest. The diamond is filled with a dark color, and the background is white.
PT. INTAN HEVEA INDUSTRY
Jalan Pulau Irian No. 13 Kawasan Industri Medan I Jalan Yos Sudarso Km 10.5. Medan 20371. INDONESIA.
Tel +62-61-6850169 +62-61-6856335 +62-61-6850168 Fax +62-61-6856335 Email intanhevea@yahoo.com
9.0 Substantial Equivalent Based on Assessment of Clinical Performance Data : Clinical data is not needed for gloves or for most devices cleared by the 510k
process.
10.0 Conclusion :
It can be concluded that the data of Powder Free Latex Examination Gloves, Non Sterile (contains 50 micrograms/dm² or less of total water extractable protein) meets ASTM Standards and FDA requirements for water leak test. No skin irritation and skin sensitization detected during the animal study. The data demonstrates Substantially Equivalent and perform as safe, as effective as well as currently marketed devices or predicated device.
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Image /page/3/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized caduceus symbol, which is a staff with two snakes coiled around it, representing medicine and healing. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the caduceus. The logo is black and white.
DEPARTMENT OF HEALTH & HUMAN SERVICES
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
NOV - 4 2011
Mr. Darwin Tandjo Factory Manager PT. INTAN HEVEA INDUSTRY Jalan Pulau Irian No.13 Kawasan Industri Medan I Jalan Yos Sudarso Km 10.5. Medan 20371 INDONESIA
Re: K111923
Trade/Device Name: POWDER FREE LATEX EXAMINATION GLOVES, NON
STERILE
(contains 50 micrograms/dm2 or less of total water extractable protein per gram).
Regulation Number: 21 CFR 880.6250
Regulation Name: Patient Examination Glove
Regulatory Class: I
Product Code: LYY
Dated: October 7, 2011
Received: October 11, 2011
Dear Mr. Tandjo:
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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
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.
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Page 2 - Mr. Tandjo
Please be advised that FDA's issuance of a substantial equivalence determination docs 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); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); 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.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices /ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
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) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm.
Sincerely yours.
Anthony, V. Newton
Anthony D. Watson, B.S., M.S., M.B.A. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Jalan Pulau Irian No. 13 Kawasan Industri Medan I Jalan Yos Sudarso Km 10.5. Medan 20371. INDONESIA
Te 62-61-6856335 62-61-6850168 Fax 62-61-6856335 Email intanhevea@vahoo.com
INDICATIONS FOR USE.
Applicant
: PT. Intan Hevea Industry.
KITI 1923 510(k) Number (if known)
Device Name : Powder Free Latex Examination Gloves, Non Sterile (contains 50 micrograms/dm2 or less of total water extractable protein per gram).
Indications for Use :
Powder Free Latex Examination Gloves, Non Sterile (contains 50 micrograms/dm² or less of total water extractable protein) is a disposable device and made of Natural Rubber Latex intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner.
Prescription Use (Per 21 CFR 801 Subpart D)
V AND/ OR Over-The-Counter Use . (Per 21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON OTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Egilut F. Oanini-Well
(Signature)
(Division Sign-Off) Division of Anesthesiology, General Hospital Infection Control, Dental Devices
510(k) Number:
§ 880.6250 Non-powdered patient examination glove.
(a)
Identification. A non-powdered patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner. A non-powdered patient examination glove does not incorporate powder for purposes other than manufacturing. The final finished glove includes only residual powder from manufacturing.(b)
Classification. Class I (general controls). The device, when it is a finger cot, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 880.9.