COMPAX MODEL 40, 400, 400T
K-Number: K884930 · 1988-12-22
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Device Summary
Frequently Asked Questions
What is the COMPAX MODEL 40, 400, 400T?
COMPAX MODEL 40, 400, 400T is a medical device that received FDA 510(k) clearance on 1988-12-22. The listed applicant is General Electric Co.. The 510(k) number is K884930.
When did COMPAX MODEL 40, 400, 400T receive FDA 510(k) clearance?
COMPAX MODEL 40, 400, 400T received FDA 510(k) clearance on 1988-12-22, under 510(k) number K884930.
Who is the listed applicant for COMPAX MODEL 40, 400, 400T?
The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMPAX MODEL 40, 400, 400T?
The FDA product code for COMPAX MODEL 40, 400, 400T is IZZ.
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 General Electric 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: IZZ)
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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