SOLOS EYESITE SPONGES
K-Number: K872612 · 1987-07-31
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Device Summary
Frequently Asked Questions
What is the SOLOS EYESITE SPONGES?
SOLOS EYESITE SPONGES is a medical device that received FDA 510(k) clearance on 1987-07-31. The listed applicant is Solos Ophthalmology. The 510(k) number is K872612.
When did SOLOS EYESITE SPONGES receive FDA 510(k) clearance?
SOLOS EYESITE SPONGES received FDA 510(k) clearance on 1987-07-31, under 510(k) number K872612.
Who is the listed applicant for SOLOS EYESITE SPONGES?
The FDA 510(k) record lists Solos Ophthalmology as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOLOS EYESITE SPONGES?
The FDA product code for SOLOS EYESITE SPONGES is HOZ.
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 Solos Ophthalmology 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: HOZ)
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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