VIEWER, RECLINING, BK-4089
K-Number: K760288 · 1976-09-08
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Device Summary
Frequently Asked Questions
What is the VIEWER, RECLINING, BK-4089?
VIEWER, RECLINING, BK-4089 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 K760288.
When did VIEWER, RECLINING, BK-4089 receive FDA 510(k) clearance?
VIEWER, RECLINING, BK-4089 received FDA 510(k) clearance on 1976-09-08, under 510(k) number K760288.
Who is the listed applicant for VIEWER, RECLINING, BK-4089?
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 VIEWER, RECLINING, BK-4089?
The FDA product code for VIEWER, RECLINING, BK-4089 is ILT.
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: ILT)
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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