FLORET OPHTHALMIC EYE SPEAR
K-Number: K830262 · 1983-04-06
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Device Summary
Frequently Asked Questions
What is the FLORET OPHTHALMIC EYE SPEAR?
FLORET OPHTHALMIC EYE SPEAR is a medical device that received FDA 510(k) clearance on 1983-04-06. The listed applicant is Ritmed, Inc.. The 510(k) number is K830262.
When did FLORET OPHTHALMIC EYE SPEAR receive FDA 510(k) clearance?
FLORET OPHTHALMIC EYE SPEAR received FDA 510(k) clearance on 1983-04-06, under 510(k) number K830262.
Who is the listed applicant for FLORET OPHTHALMIC EYE SPEAR?
The FDA 510(k) record lists Ritmed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLORET OPHTHALMIC EYE SPEAR?
The FDA product code for FLORET OPHTHALMIC EYE SPEAR 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 Ritmed, Inc. 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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