IMPREGUM-F
K-Number: K853529 · 1986-03-17
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Device Summary
Frequently Asked Questions
What is the IMPREGUM-F?
IMPREGUM-F is a medical device that received FDA 510(k) clearance on 1986-03-17. The listed applicant is Espe GmbH (Us). The 510(k) number is K853529.
When did IMPREGUM-F receive FDA 510(k) clearance?
IMPREGUM-F received FDA 510(k) clearance on 1986-03-17, under 510(k) number K853529.
Who is the listed applicant for IMPREGUM-F?
The FDA 510(k) record lists Espe GmbH (Us) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IMPREGUM-F?
The FDA product code for IMPREGUM-F is ELW.
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 Espe GmbH (Us) 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: ELW)
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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