EBS POWDER
K-Number: K820928 · 1982-04-21
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Device Summary
Frequently Asked Questions
What is the EBS POWDER?
EBS POWDER is a medical device that received FDA 510(k) clearance on 1982-04-21. The listed applicant is Dutchland Laboratories, Inc.. The 510(k) number is K820928.
When did EBS POWDER receive FDA 510(k) clearance?
EBS POWDER received FDA 510(k) clearance on 1982-04-21, under 510(k) number K820928.
Who is the listed applicant for EBS POWDER?
The FDA 510(k) record lists Dutchland Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EBS POWDER?
The FDA product code for EBS POWDER is KIP.
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 Dutchland 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: KIP)
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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