POROPLAST-EYE DRESSING
K-Number: K802786 · 1980-12-17
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Device Summary
Frequently Asked Questions
What is the POROPLAST-EYE DRESSING?
POROPLAST-EYE DRESSING is a medical device that received FDA 510(k) clearance on 1980-12-17. The listed applicant is Secol Co.. The 510(k) number is K802786.
When did POROPLAST-EYE DRESSING receive FDA 510(k) clearance?
POROPLAST-EYE DRESSING received FDA 510(k) clearance on 1980-12-17, under 510(k) number K802786.
Who is the listed applicant for POROPLAST-EYE DRESSING?
The FDA 510(k) record lists Secol Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POROPLAST-EYE DRESSING?
The FDA product code for POROPLAST-EYE DRESSING is HOY.
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 Secol Co. 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: HOY)
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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