FEMOSTOP II
K-Number: K944259 · 1995-07-20
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Device Summary
Frequently Asked Questions
What is the FEMOSTOP II?
FEMOSTOP II is a medical device that received FDA 510(k) clearance on 1995-07-20. The listed applicant is Radi Medical Systems AB. The 510(k) number is K944259.
When did FEMOSTOP II receive FDA 510(k) clearance?
FEMOSTOP II received FDA 510(k) clearance on 1995-07-20, under 510(k) number K944259.
Who is the listed applicant for FEMOSTOP II?
The FDA 510(k) record lists Radi Medical Systems AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FEMOSTOP II?
The FDA product code for FEMOSTOP II is DXC.
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 Radi Medical Systems AB 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: DXC)
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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