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FDA 510(k)

ECHOVACS

K-Number: K971776 · 1997-07-14

ApplicantVmi Technologies
Decision Date1997-07-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ECHOVACS is the device name listed in this FDA 510(k) record. The listed applicant is Vmi Technologies. It received FDA 510(k) clearance on 1997-07-14 under 510(k) number K971776. 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 ECHOVACS?

ECHOVACS is a medical device that received FDA 510(k) clearance on 1997-07-14. The listed applicant is Vmi Technologies. The 510(k) number is K971776.

When did ECHOVACS receive FDA 510(k) clearance?

ECHOVACS received FDA 510(k) clearance on 1997-07-14, under 510(k) number K971776.

Who is the listed applicant for ECHOVACS?

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

What is the FDA product code for ECHOVACS?

The FDA product code for ECHOVACS is LLZ.

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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.

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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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