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FDA 510(k)

ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000

K-Number: K984405 · 1999-02-08

Decision Date1999-02-08
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000 is the device name listed in this FDA 510(k) record. The listed applicant is Intracom Corp.. It received FDA 510(k) clearance on 1999-02-08 under 510(k) number K984405. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000?

ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000 is a medical device that received FDA 510(k) clearance on 1999-02-08. The listed applicant is Intracom Corp.. The 510(k) number is K984405.

When did ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000 receive FDA 510(k) clearance?

ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000 received FDA 510(k) clearance on 1999-02-08, under 510(k) number K984405.

Who is the listed applicant for ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000?

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

What is the FDA product code for ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000?

The FDA product code for ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000 is LMB.

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: LMB)

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

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