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FDA 510(k)

ECHO-OIL

K-Number: K781631 · 1978-10-10

Decision Date1978-10-10
Product CodeEMX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ECHO-OIL is the device name listed in this FDA 510(k) record. The listed applicant is Echo Laboratories, Inc.. It received FDA 510(k) clearance on 1978-10-10 under 510(k) number K781631. The device is classified under product code EMX. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECHO-OIL?

ECHO-OIL is a medical device that received FDA 510(k) clearance on 1978-10-10. The listed applicant is Echo Laboratories, Inc.. The 510(k) number is K781631.

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

ECHO-OIL received FDA 510(k) clearance on 1978-10-10, under 510(k) number K781631.

Who is the listed applicant for ECHO-OIL?

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

What is the FDA product code for ECHO-OIL?

The FDA product code for ECHO-OIL is EMX.

Other records listing Echo Laboratories, Inc. 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: EMX)

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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