DESK, BEANBAG SHUFFLE, BK-6059
K-Number: K760292 · 1976-09-08
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Device Summary
Frequently Asked Questions
What is the DESK, BEANBAG SHUFFLE, BK-6059?
DESK, BEANBAG SHUFFLE, BK-6059 is a medical device that received FDA 510(k) clearance on 1976-09-08. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K760292.
When did DESK, BEANBAG SHUFFLE, BK-6059 receive FDA 510(k) clearance?
DESK, BEANBAG SHUFFLE, BK-6059 received FDA 510(k) clearance on 1976-09-08, under 510(k) number K760292.
Who is the listed applicant for DESK, BEANBAG SHUFFLE, BK-6059?
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 DESK, BEANBAG SHUFFLE, BK-6059?
The FDA product code for DESK, BEANBAG SHUFFLE, BK-6059 is KNO.
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: KNO)
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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