SEDATELEC ASP ACUPUNCTURE NEEDLES
K-Number: K983798 · 1999-08-27
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Device Summary
Frequently Asked Questions
What is the SEDATELEC ASP ACUPUNCTURE NEEDLES?
SEDATELEC ASP ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 1999-08-27. The listed applicant is Sedatelec. The 510(k) number is K983798.
When did SEDATELEC ASP ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?
SEDATELEC ASP ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 1999-08-27, under 510(k) number K983798.
Who is the listed applicant for SEDATELEC ASP ACUPUNCTURE NEEDLES?
The FDA 510(k) record lists Sedatelec as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SEDATELEC ASP ACUPUNCTURE NEEDLES?
The FDA product code for SEDATELEC ASP 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 Sedatelec 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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