BK-1544 BE OK SCOOP DISK
K-Number: K800019 · 1980-01-21
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Device Summary
Frequently Asked Questions
What is the BK-1544 BE OK SCOOP DISK?
BK-1544 BE OK SCOOP DISK is a medical device that received FDA 510(k) clearance on 1980-01-21. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K800019.
When did BK-1544 BE OK SCOOP DISK receive FDA 510(k) clearance?
BK-1544 BE OK SCOOP DISK received FDA 510(k) clearance on 1980-01-21, under 510(k) number K800019.
Who is the listed applicant for BK-1544 BE OK SCOOP DISK?
The FDA 510(k) record lists Fred Sammons, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BK-1544 BE OK SCOOP DISK?
The FDA product code for BK-1544 BE OK SCOOP DISK is ILC.
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 Fred Sammons, 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: ILC)
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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