FDA 510(k)

ECHO, MODEL MM-1000

K-Number: K821383 · 1982-06-23

Decision Date1982-06-23

Product CodeLIF

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

ECHO, MODEL MM-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Mesa Medical, Inc.. It received FDA 510(k) clearance on 1982-06-23 under 510(k) number K821383. The device is classified under product code LIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECHO, MODEL MM-1000?

ECHO, MODEL MM-1000 is a medical device that received FDA 510(k) clearance on 1982-06-23. The listed applicant is Mesa Medical, Inc.. The 510(k) number is K821383.

When did ECHO, MODEL MM-1000 receive FDA 510(k) clearance?

ECHO, MODEL MM-1000 received FDA 510(k) clearance on 1982-06-23, under 510(k) number K821383.

Who is the listed applicant for ECHO, MODEL MM-1000?

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

What is the FDA product code for ECHO, MODEL MM-1000?

The FDA product code for ECHO, MODEL MM-1000 is LIF.

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Other records listing Mesa Medical, Inc. as applicant

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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.