BK-1472 SPATULA SPOON
K-Number: K790170 · 1979-02-13
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Device Summary
Frequently Asked Questions
What is the BK-1472 SPATULA SPOON?
BK-1472 SPATULA SPOON is a medical device that received FDA 510(k) clearance on 1979-02-13. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K790170.
When did BK-1472 SPATULA SPOON receive FDA 510(k) clearance?
BK-1472 SPATULA SPOON received FDA 510(k) clearance on 1979-02-13, under 510(k) number K790170.
Who is the listed applicant for BK-1472 SPATULA SPOON?
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-1472 SPATULA SPOON?
The FDA product code for BK-1472 SPATULA SPOON 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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