MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.O ATTACH
K-Number: K870840 · 1987-06-12
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Device Summary
Frequently Asked Questions
What is the MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.O ATTACH?
MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.O ATTACH is a medical device that received FDA 510(k) clearance on 1987-06-12. The listed applicant is Directed Energy, Inc.. The 510(k) number is K870840.
When did MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.O ATTACH receive FDA 510(k) clearance?
MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.O ATTACH received FDA 510(k) clearance on 1987-06-12, under 510(k) number K870840.
Who is the listed applicant for MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.O ATTACH?
The FDA 510(k) record lists Directed Energy, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.O ATTACH?
The FDA product code for MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.O ATTACH is EWG.
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.
Other records listing Directed Energy, 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: EWG)
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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