FERRIS TRANSPARENT WOUND DRESSING W/HYDROCOLLOID
K-Number: K871675 · 1987-08-06
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Device Summary
Frequently Asked Questions
What is the FERRIS TRANSPARENT WOUND DRESSING W/HYDROCOLLOID?
FERRIS TRANSPARENT WOUND DRESSING W/HYDROCOLLOID is a medical device that received FDA 510(k) clearance on 1987-08-06. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K871675.
When did FERRIS TRANSPARENT WOUND DRESSING W/HYDROCOLLOID receive FDA 510(k) clearance?
FERRIS TRANSPARENT WOUND DRESSING W/HYDROCOLLOID received FDA 510(k) clearance on 1987-08-06, under 510(k) number K871675.
Who is the listed applicant for FERRIS TRANSPARENT WOUND DRESSING W/HYDROCOLLOID?
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 TRANSPARENT WOUND DRESSING W/HYDROCOLLOID?
The FDA product code for FERRIS TRANSPARENT WOUND DRESSING W/HYDROCOLLOID 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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