VISI-SWAB OPHTALMIC SPONGE
K-Number: K902750 · 1990-07-26
Advertisement
Device Summary
Frequently Asked Questions
What is the VISI-SWAB OPHTALMIC SPONGE?
VISI-SWAB OPHTALMIC SPONGE is a medical device that received FDA 510(k) clearance on 1990-07-26. The listed applicant is Visitec Co.. The 510(k) number is K902750.
When did VISI-SWAB OPHTALMIC SPONGE receive FDA 510(k) clearance?
VISI-SWAB OPHTALMIC SPONGE received FDA 510(k) clearance on 1990-07-26, under 510(k) number K902750.
Who is the listed applicant for VISI-SWAB OPHTALMIC SPONGE?
The FDA 510(k) record lists Visitec Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VISI-SWAB OPHTALMIC SPONGE?
The FDA product code for VISI-SWAB OPHTALMIC SPONGE 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 Visitec 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: 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.
Advertisement