ECHO-OIL
K-Number: K781631 · 1978-10-10
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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