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FDA 510(k)

VIEWER, RECLINING, BK-4089

K-Number: K760288 · 1976-09-08

Decision Date1976-09-08
Product CodeILT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VIEWER, RECLINING, BK-4089 is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1976-09-08 under 510(k) number K760288. The device is classified under product code ILT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 278 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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