FERRIS HYDROPHILIC DRESSING
K-Number: K880330 · 1988-03-23
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Device Summary
Frequently Asked Questions
What is the FERRIS HYDROPHILIC DRESSING?
FERRIS HYDROPHILIC DRESSING is a medical device that received FDA 510(k) clearance on 1988-03-23. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K880330.
When did FERRIS HYDROPHILIC DRESSING receive FDA 510(k) clearance?
FERRIS HYDROPHILIC DRESSING received FDA 510(k) clearance on 1988-03-23, under 510(k) number K880330.
Who is the listed applicant for FERRIS HYDROPHILIC DRESSING?
The FDA 510(k) record lists Ferris Mfg. Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FERRIS HYDROPHILIC DRESSING?
The FDA product code for FERRIS HYDROPHILIC DRESSING is FRO. This falls under the Anesthesiology category.
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 Ferris Mfg. 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: FRO)
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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