PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES
K-Number: K905462 · 1991-02-06
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Device Summary
Frequently Asked Questions
What is the PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES?
PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES is a medical device that received FDA 510(k) clearance on 1991-02-06. The listed applicant is Angiosystems, Inc.. The 510(k) number is K905462.
When did PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES receive FDA 510(k) clearance?
PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES received FDA 510(k) clearance on 1991-02-06, under 510(k) number K905462.
Who is the listed applicant for PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES?
The FDA 510(k) record lists Angiosystems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES?
The FDA product code for PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES is LRP.
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 Angiosystems, 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: LRP)
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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