SUPRA AP CHOICE 83
K-Number: K833280 · 1983-12-26
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Device Summary
Frequently Asked Questions
What is the SUPRA AP CHOICE 83?
SUPRA AP CHOICE 83 is a medical device that received FDA 510(k) clearance on 1983-12-26. The listed applicant is Genesis Industries, Inc.. The 510(k) number is K833280.
When did SUPRA AP CHOICE 83 receive FDA 510(k) clearance?
SUPRA AP CHOICE 83 received FDA 510(k) clearance on 1983-12-26, under 510(k) number K833280.
Who is the listed applicant for SUPRA AP CHOICE 83?
The FDA 510(k) record lists Genesis Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUPRA AP CHOICE 83?
The FDA product code for SUPRA AP CHOICE 83 is EIS.
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 Genesis Industries, 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: EIS)
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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