EDEC 90C
K-Number: K875342 · 1988-01-29
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Device Summary
Frequently Asked Questions
What is the EDEC 90C?
EDEC 90C is a medical device that received FDA 510(k) clearance on 1988-01-29. The listed applicant is Electromed Intl., Ltd.. The 510(k) number is K875342.
When did EDEC 90C receive FDA 510(k) clearance?
EDEC 90C received FDA 510(k) clearance on 1988-01-29, under 510(k) number K875342.
Who is the listed applicant for EDEC 90C?
The FDA 510(k) record lists Electromed Intl., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EDEC 90C?
The FDA product code for EDEC 90C is IZO.
Other records listing Electromed Intl., Ltd. 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: IZO)
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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