HYCURE
K-Number: K955506 · 1996-01-17
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Device Summary
Frequently Asked Questions
What is the HYCURE?
HYCURE is a medical device that received FDA 510(k) clearance on 1996-01-17. The listed applicant is The Hymed Group Corp.. The 510(k) number is K955506.
When did HYCURE receive FDA 510(k) clearance?
HYCURE received FDA 510(k) clearance on 1996-01-17, under 510(k) number K955506.
Who is the listed applicant for HYCURE?
The FDA 510(k) record lists The Hymed Group Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HYCURE?
The FDA product code for HYCURE is KGN.
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 The Hymed Group 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: KGN)
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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