KHT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE

K980469 · American Institute of Koryo Hand Therapy · MQX · Apr 3, 1998 · General Hospital

Device Facts

• Record ID: K980469
• Device Name: KHT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE
• Applicant: American Institute of Koryo Hand Therapy
• Product Code: MQX · General Hospital
• Decision Date: Apr 3, 1998
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 880.5580
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

Acupuncture needles are defined as prescription devices intended to pierce the skin in the practice of acupuncture by qualified practitioners of acupuncture as determined by the States.

Device Story

KHT Sooji Needle is a sterile, single-use acupuncture needle designed for hand acupuncture. The device is used by qualified acupuncture practitioners to pierce the skin during acupuncture therapy. It functions as a manual instrument to stimulate specific points on the hand. The device is provided sterile and is intended for one-time use to ensure patient safety and prevent cross-contamination. It is used in clinical settings by licensed professionals to support acupuncture treatment protocols.

Clinical Evidence

No clinical data. The submission relies on the device's design, material composition, sterility, and biocompatibility to demonstrate substantial equivalence to legally marketed predicate devices.

Technological Characteristics

Sterile, single-use acupuncture needle. Materials and design meet general specifications for acupuncture needles. Sterilization is implied as a requirement for single-use status.

Indications for Use

Indicated for use by qualified acupuncture practitioners to pierce the skin for the practice of acupuncture.

Regulatory Classification

Identification

An acupuncture needle is a device intended to pierce the skin in the practice of acupuncture. The device consists of a solid, stainless steel needle. The device may have a handle attached to the needle to facilitate the delivery of acupuncture treatment.

Special Controls

*Classification.* Class II (special controls). The device, when it is an acupuncture point locator or a single use acupuncture needle, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 880.9. Acupuncture needles must comply with the following special controls:(1) Labeling for single use only and conformance to the requirements for prescription devices set out in 21 CFR 801.109, (2) Device material biocompatibility, and (3) Device sterility.

Predicate Devices

• CW-Disposable Acupuncture Needle (K962419)

Submission Summary (Full Text)

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800JI NEEDLE

K 980469

## American Institute of Koryo Hand Therapy, Inc.

3435 Wilshire Blvd., Suite 690, Los Angeles, CA 90010 Tel: [phone] Fax: [phone]

Premarket Notification [510(k) Number]:

## 510(k) SUMMARY As Required by 21 CFR 807.92(c)

| Trade Name: | KHT Sooji Needle |
|----------------------|------------------------------------------|
| Common Name: | Hand Acupuncture Needles |
| Classification Name: | Class II, Single use acupuncture needles |

Legally Marketed Device to Which We Are Claiming Equivalence: CW-Disposable Acupuncture Needle 510(k) Document Number: K962419

Acupuncture needles are defined as prescription devices intended to pierce the skin in the practice of acupuncture by qualified practitioners of acupuncture as determined by the States.

Acupuncture needles have been used for the general practice of acupuncture in the United States for over 30 years. Since that time, we are not aware of any serious or life threatening accidents involving acupuncture needles.

Acupuncture needles which were sold through commercial interstate distribution prior to May 28, 1976 were non-sterile, reusable acupuncture needles. Acupuncture needles which are currently being marketed through interstate distribution (i.e., 1997) offer greater safety since they are sterlilized, single use only acupuncture needles.

The subject of this 510(k) application - the KHT Sooji Needle - is a sterilized, single use only hand acupuncture needle. The design, material used, sterility and biocompatibility of this acupuncture needle meet the general specifications and criteria for an single use acupuncture needle and is effective for the practice of acupuncture.

In conclusion, based on the information provided with this 510(k) application, the KHT Sooji Needle meets the criteria for 510(k) acceptance. The KHT Sooji Needle is equivalent to acupuncture needles which were in commercial distribution prior to May 28, 1976. Also, the KHT Sooji Needle is equivalent to other single use acupuncture needles which are currently being sold through interstate commerce.

Jin Hae Lew, Director

22-98 Date

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Image /page/1/Picture/1 description: The image shows the logo for the Department of Health & Human Services - USA. The logo consists of a stylized eagle with three lines forming its body and wings. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion around the eagle.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

3 APR

American Institute of Koryo Hand Therapy, Incorporated C/O Mr. George Su Requlatory Consultant Crosslinks International 17870 Castleton Street, Suite 265 Industry, California 91748

Re : K980469 KHT Sooji Needle, Hand Acupuncture Needles Trade Name: Requlatory Class: II Product Code: MQX Dated: January 22, 1998 Received: February 6, 1998

Dear Mr. Su:

We have reviewed your Section 510 (k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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, Druq, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions The general controls provisions of the Act 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 (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Requlations, Title 21, Parts 800 to 895. ਬੈ substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) regulation (21 CFR Part 820) and that, through periodic GMP inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in Please note: this response to your the Federal Reqister. premarket notification submission does not affect any obligation you might have under sections 531 through 542 of

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Page 2 - Mr. Su

the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.

This letter will allow you to begin marketing your device as described in your 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 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number [phone] or [phone] or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".

Sincerely yours,

Timothy A. Ulatowski

Timo Directbr Division of Dental, Infection Control, and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

.
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## Indications For Use

510(k) Number ( if known )

KHT Sooji Needle, Hand Acupuncture Needle Device Name: _

Indications For Use:

To pierce the skin in the practice of acupuncture by qualified practitioners of acupuncture as determined by the states.

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

Concurrence of CDRH, Office of Device Evaluation ( ODE )

Patrica Crescent
(Division Sign-Off)

(Li

- Division of Dental, Infection Copntrol, and General Hospital Devi D
c.
510(k) Number K980469
510(k. ....

Prescription Use ***_***_ OR Over-The-Counter Use ***_***_

( Optional Format 1-2-96 )

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