PORTASCOOT POWER SEAT
K-Number: K840866 · 1984-03-19
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Device Summary
Frequently Asked Questions
What is the PORTASCOOT POWER SEAT?
PORTASCOOT POWER SEAT is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is E.F. Brewer Co.. The 510(k) number is K840866.
When did PORTASCOOT POWER SEAT receive FDA 510(k) clearance?
PORTASCOOT POWER SEAT received FDA 510(k) clearance on 1984-03-19, under 510(k) number K840866.
Who is the listed applicant for PORTASCOOT POWER SEAT?
The FDA 510(k) record lists E.F. Brewer Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PORTASCOOT POWER SEAT?
The FDA product code for PORTASCOOT POWER SEAT is INI.
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 E.F. Brewer Co. 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: INI)
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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