(407 days)
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No
The document describes a standard TENS device and does not mention any AI or ML components or capabilities.
Yes
The device is described as a transcutaneous electrical nerve stimulator for symptomatic pain relief, which is a therapeutic purpose.
No
The device description states its purpose is for "symptomatic pain relief" by applying electrical current, which is a therapeutic function, not a diagnostic one. It does not mention analyzing or identifying a condition.
No
The device description explicitly states it is a "battery operated portable transcutaneous electrical nerve stimulator," which is a hardware device.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are medical devices used to examine specimens taken from the human body (like blood, urine, tissue) to provide information about a person's health. This testing is done outside of the body (in vitro).
- Panag Function: The description clearly states the "Panag" applies an electrical current through electrodes to a patient's skin. This is a direct application to the body, not the testing of a specimen taken from the body.
The "Panag" is a therapeutic device used for pain relief, not a diagnostic device used for testing samples.
N/A
Intended Use / Indications for Use
The "Panag" is a battery operated portable transcutaneous electrical nerve stimulator used to apply an electrical current through electrodes to a patient's skin for symptomatic pain relief. For the symptomatic relief of chronic intractable, post-traumatic and post-surgical pain.
Product codes
GZJ
Device Description
The "Panag" is a battery operated portable transcutaneous electrical nerve stimulator used to apply an electrical current through electrodes to a patient's skin for symptomatic pain relief.
Mentions image processing
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Mentions AI, DNN, or ML
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Input Imaging Modality
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Anatomical Site
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Indicated Patient Age Range
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Intended User / Care Setting
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Description of the training set, sample size, data source, and annotation protocol
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Description of the test set, sample size, data source, and annotation protocol
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Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
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Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
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Predicate Device(s)
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Reference Device(s)
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Predetermined Change Control Plan (PCCP) - All Relevant Information
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§ 882.5890 Transcutaneous electrical nerve stimulator for pain relief.
(a)
Identification. A transcutaneous electrical nerve stimulator for pain relief is a device used to apply an electrical current to electrodes on a patient's skin to treat pain.(b)
Classification. Class II (performance standards).
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Image /page/0/Picture/1 description: The image is a seal for the Department of Health & Human Services USA. The seal is circular and contains the words "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" around the perimeter. In the center of the seal is an abstract image of an eagle.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
JUL 3 0 2002
Mr. Peter Kalabakas Panag International 43 Derby Road Bertrams Johannesburg South Africa 2094
Re: K011891 Trade/Device Name: Panag Regulation Number: 882.5890 Regulation Name: Transcutaneous Electrical Nerve Stimulator For Pain Relief Regulatory Class: Class II Product Code: GZJ Dated: May 27, 2002 Received: June 10, 2002
Dear Mr. Kalabakas:
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 (PMA), 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.
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.
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Page 2 - Mr. Peter Kalabakas
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 and additionally 21 CFR Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4659. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained 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/dsma/dsmamain.html
Sincerely vours.
- Mark A. Millhuser
Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
2
INDICATION FOR USE STATEMENT
K 011891 510(k) Number (if known):
Panag
Device Name:
Indication for Use:
The "Panag" is a battery operated portable transcutaneous electrical nerve stimulator used to apply an electrical current through electrodes to a patient's skin for symptomatic pain relief.
For the symptomatic relief of chronic intractable, post-traumatic and post-surgical pain.
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use
(Per 21 CFR 801.109)
Division Sign-Off
and Neurological Devices
OR
Over-The-Counter Use
ﺔ ﺑﺎﺳ
(Optional Format 1-2-96)
2-2
:
510(k) Number -
Division of General. Restorative