DBC ACUPUNTURE NEEDLES(SEVERAL TYPES ARE DESCRIBED ON THE FOLLOWING PAGES)
Device Facts
| Record ID | K963300 |
|---|---|
| Device Name | DBC ACUPUNTURE NEEDLES(SEVERAL TYPES ARE DESCRIBED ON THE FOLLOWING PAGES) |
| Applicant | Lhasa Medical, Inc. |
| Product Code | MQX · General Hospital |
| Decision Date | Sep 23, 1996 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 880.5580 |
| Device Class | Class 2 |
| Attributes | Therapeutic |
Intended Use
Acupuncture needles are defined as devices intended to pierce the skin in the practice of acupuncture by qualified practitioners or acupuncture as determined by the States.
Device Story
DBC acupuncture needle; sterile, single-use device; intended for skin piercing during acupuncture practice. Operated by qualified practitioners in clinical settings. Device design follows general specifications for acupuncture needles. No reported accidents or failures since 1986. Benefits include enhanced safety compared to historical non-sterile, reusable needles.
Clinical Evidence
No clinical data; safety established through historical usage since 1986 with no reported accidents or device failures.
Technological Characteristics
Sterile, single-use acupuncture needle. Meets general specifications for acupuncture needles.
Indications for Use
Indicated for use by qualified practitioners 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.
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