MICRO-X 100CP
K-Number: K884134 · 1988-10-21
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Device Summary
Frequently Asked Questions
What is the MICRO-X 100CP?
MICRO-X 100CP is a medical device that received FDA 510(k) clearance on 1988-10-21. The listed applicant is Fischer Imaging Corp.. The 510(k) number is K884134.
When did MICRO-X 100CP receive FDA 510(k) clearance?
MICRO-X 100CP received FDA 510(k) clearance on 1988-10-21, under 510(k) number K884134.
Who is the listed applicant for MICRO-X 100CP?
The FDA 510(k) record lists Fischer Imaging Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO-X 100CP?
The FDA product code for MICRO-X 100CP is IZO.
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 Fischer Imaging Corp. 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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