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FDA 510(k)

ASP TITANIUM

K-Number: K060392 · 2006-04-26

ApplicantSedatelec
Decision Date2006-04-26
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ASP TITANIUM is the device name listed in this FDA 510(k) record. The listed applicant is Sedatelec. It received FDA 510(k) clearance on 2006-04-26 under 510(k) number K060392. 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 ASP TITANIUM?

ASP TITANIUM is a medical device that received FDA 510(k) clearance on 2006-04-26. The listed applicant is Sedatelec. The 510(k) number is K060392.

When did ASP TITANIUM receive FDA 510(k) clearance?

ASP TITANIUM received FDA 510(k) clearance on 2006-04-26, under 510(k) number K060392.

Who is the listed applicant for ASP TITANIUM?

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 ASP TITANIUM?

The FDA product code for ASP TITANIUM 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.

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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.

K101267PREMIO 10 MOXAK983800DN ACUPUNTURE NEEDLESK983798SEDATELEC ASP ACUPUNCTURE NEEDLES

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.

K162566AIK Sterile Acupuncture Needles for Single UseChangchun Aik Medical Devices Co., Ltd.K132896CJ-TYPE: METAL HANDLE WITH GUIDE TUBE, PJ-TYPE: PLASTIC HANDLE WITH GUIDE TUBE, CB-TYPE: METAL HANDLE WITHOUT GUIDE TUBEAsia-Med GmbH and CO KGK111392WOOJEON ACUPUNCTURE NEEDLE (=SERA ACUPUNCTURE NEEDLE)Woojeon CompanyK103061BIOMATE STERILE ACUPUNCTURE NEEDLEBiomate Medical Devices Technology Co., Ltd.K092240ACUPUNCTURE NEEDLESHaenglim Seowon Medical Co.K090199JIAJIAN ACUPUNCTURE NEEDLEWuxi Jiajian Medical Instrument Co., Ltd.

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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