Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ECHOLINK

K-Number: K980060 · 1998-02-25

ApplicantMpacs, LLC
Decision Date1998-02-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ECHOLINK is the device name listed in this FDA 510(k) record. The listed applicant is Mpacs, LLC. It received FDA 510(k) clearance on 1998-02-25 under 510(k) number K980060. 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 ECHOLINK?

ECHOLINK is a medical device that received FDA 510(k) clearance on 1998-02-25. The listed applicant is Mpacs, LLC. The 510(k) number is K980060.

When did ECHOLINK receive FDA 510(k) clearance?

ECHOLINK received FDA 510(k) clearance on 1998-02-25, under 510(k) number K980060.

Who is the listed applicant for ECHOLINK?

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

What is the FDA product code for ECHOLINK?

The FDA product code for ECHOLINK 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.

Other records listing Mpacs, LLC 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: 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

View on FDA Database →

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

↑