MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USE
K-Number: K883575 · 1988-09-12
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Device Summary
Frequently Asked Questions
What is the MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USE?
MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USE is a medical device that received FDA 510(k) clearance on 1988-09-12. The listed applicant is Site Microsurgical Systems, Inc.. The 510(k) number is K883575.
When did MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USE receive FDA 510(k) clearance?
MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USE received FDA 510(k) clearance on 1988-09-12, under 510(k) number K883575.
Who is the listed applicant for MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USE?
The FDA 510(k) record lists Site Microsurgical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USE?
The FDA product code for MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USE is HMG.
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 Site Microsurgical Systems, 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: HMG)
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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