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FDA 510(k)

EXTENSIONS-LUSATZTISCH

K-Number: K812779 · 1981-10-26

ApplicantThe Telos Co.
Decision Date1981-10-26
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EXTENSIONS-LUSATZTISCH is the device name listed in this FDA 510(k) record. The listed applicant is The Telos Co.. It received FDA 510(k) clearance on 1981-10-26 under 510(k) number K812779. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENSIONS-LUSATZTISCH?

EXTENSIONS-LUSATZTISCH is a medical device that received FDA 510(k) clearance on 1981-10-26. The listed applicant is The Telos Co.. The 510(k) number is K812779.

When did EXTENSIONS-LUSATZTISCH receive FDA 510(k) clearance?

EXTENSIONS-LUSATZTISCH received FDA 510(k) clearance on 1981-10-26, under 510(k) number K812779.

Who is the listed applicant for EXTENSIONS-LUSATZTISCH?

The FDA 510(k) record lists The Telos Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXTENSIONS-LUSATZTISCH?

The FDA product code for EXTENSIONS-LUSATZTISCH is HST.

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 The Telos Co. 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.

K812778THE TELOS EQUIPMENT

Related Devices (Code: HST)

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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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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