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FDA 510(k)

TEL-ECHO SYSTEM

K-Number: K990052 · 1999-02-19

Decision Date1999-02-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TEL-ECHO SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Solutions, Inc.. It received FDA 510(k) clearance on 1999-02-19 under 510(k) number K990052. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEL-ECHO SYSTEM?

TEL-ECHO SYSTEM is a medical device that received FDA 510(k) clearance on 1999-02-19. The listed applicant is Innovative Medical Solutions, Inc.. The 510(k) number is K990052.

When did TEL-ECHO SYSTEM receive FDA 510(k) clearance?

TEL-ECHO SYSTEM received FDA 510(k) clearance on 1999-02-19, under 510(k) number K990052.

Who is the listed applicant for TEL-ECHO SYSTEM?

The FDA 510(k) record lists Innovative Medical Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEL-ECHO SYSTEM?

The FDA product code for TEL-ECHO SYSTEM is LLZ.

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.

Related Devices (Code: LLZ)

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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