DBC PRESS ACUPUNCTURE NEEDLES
K-Number: K031250 · 2003-07-15
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Device Summary
Frequently Asked Questions
What is the DBC PRESS ACUPUNCTURE NEEDLES?
DBC PRESS ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 2003-07-15. The listed applicant is Lhasa Medical, Inc.. The 510(k) number is K031250.
When did DBC PRESS ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?
DBC PRESS ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 2003-07-15, under 510(k) number K031250.
Who is the listed applicant for DBC PRESS ACUPUNCTURE NEEDLES?
The FDA 510(k) record lists Lhasa Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DBC PRESS ACUPUNCTURE NEEDLES?
The FDA product code for DBC PRESS ACUPUNCTURE NEEDLES is MQX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Lhasa Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MQX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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