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FDA 510(k)

THE TELOS EQUIPMENT

K-Number: K812778 · 1981-12-08

ApplicantThe Telos Co.
Decision Date1981-12-08
Product CodeKQW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE TELOS EQUIPMENT 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 1981-12-08 under 510(k) number K812778. The device is classified under product code KQW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE TELOS EQUIPMENT?

THE TELOS EQUIPMENT is a medical device that received FDA 510(k) clearance on 1981-12-08. The listed applicant is The Telos Co.. The 510(k) number is K812778.

When did THE TELOS EQUIPMENT receive FDA 510(k) clearance?

THE TELOS EQUIPMENT received FDA 510(k) clearance on 1981-12-08, under 510(k) number K812778.

Who is the listed applicant for THE TELOS EQUIPMENT?

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 THE TELOS EQUIPMENT?

The FDA product code for THE TELOS EQUIPMENT is KQW.

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.

K812779EXTENSIONS-LUSATZTISCH

Related Devices (Code: KQW)

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.

K926237O'BRIEN GONIOMETERSgarlato Laboratories, Inc.K901744DOBBHOFF(R) RETRIEVAL FORCEPSBiosearch Medical Products, Inc.K870767THE (CROM) TESTERTwin City Surgical, Inc.K850082HAND HELD GONIOMETERChattanooga Group, Inc.K831550FINGER BONIOMETER BK7506Fred Sammons, Inc.K810441UNIVERSAL GONIMETERFred Sammons, Inc.

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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