BK-6111 HI-D TRANSFER BOARD
K-Number: K813629 · 1982-01-19
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Device Summary
Frequently Asked Questions
What is the BK-6111 HI-D TRANSFER BOARD?
BK-6111 HI-D TRANSFER BOARD is a medical device that received FDA 510(k) clearance on 1982-01-19. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K813629.
When did BK-6111 HI-D TRANSFER BOARD receive FDA 510(k) clearance?
BK-6111 HI-D TRANSFER BOARD received FDA 510(k) clearance on 1982-01-19, under 510(k) number K813629.
Who is the listed applicant for BK-6111 HI-D TRANSFER BOARD?
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-6111 HI-D TRANSFER BOARD?
The FDA product code for BK-6111 HI-D TRANSFER BOARD is IKX.
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: IKX)
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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