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FDA 510(k)

SEDATELEC ASP ACUPUNCTURE NEEDLES

K-Number: K983798 · 1999-08-27

ApplicantSedatelec
Decision Date1999-08-27
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SEDATELEC ASP ACUPUNCTURE NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Sedatelec. It received FDA 510(k) clearance on 1999-08-27 under 510(k) number K983798. The device is classified under product code MQX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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