PALM BEACH SEATING SYSTEM
K-Number: K820761 · 1982-04-21
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Device Summary
Frequently Asked Questions
What is the PALM BEACH SEATING SYSTEM?
PALM BEACH SEATING SYSTEM is a medical device that received FDA 510(k) clearance on 1982-04-21. The listed applicant is Pb Sales C/O Geller & Bozeman. The 510(k) number is K820761.
When did PALM BEACH SEATING SYSTEM receive FDA 510(k) clearance?
PALM BEACH SEATING SYSTEM received FDA 510(k) clearance on 1982-04-21, under 510(k) number K820761.
Who is the listed applicant for PALM BEACH SEATING SYSTEM?
The FDA 510(k) record lists Pb Sales C/O Geller & Bozeman as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PALM BEACH SEATING SYSTEM?
The FDA product code for PALM BEACH SEATING SYSTEM is KNN.
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 Pb Sales C/O Geller & Bozeman 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: KNN)
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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