ASCON OPHTHALMIC SPONGE
K-Number: K852055 · 1985-09-04
Device Summary
Frequently Asked Questions
What is the ASCON OPHTHALMIC SPONGE?
ASCON OPHTHALMIC SPONGE is a medical device that received FDA 510(k) clearance on 1985-09-04. The listed applicant is Ascon Medical Instruments, Ltd.. The 510(k) number is K852055.
When did ASCON OPHTHALMIC SPONGE receive FDA 510(k) clearance?
ASCON OPHTHALMIC SPONGE received FDA 510(k) clearance on 1985-09-04, under 510(k) number K852055.
Who is the listed applicant for ASCON OPHTHALMIC SPONGE?
The FDA 510(k) record lists Ascon Medical Instruments, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASCON OPHTHALMIC SPONGE?
The FDA product code for ASCON OPHTHALMIC 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 Ascon Medical Instruments, Ltd. 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.