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FDA 510(k)

MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USE

K-Number: K883575 · 1988-09-12

Decision Date1988-09-12
Product CodeHMG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MODIFIED SITE MOBILE STAND FOR OPHTHALMIC USE is the device name listed in this FDA 510(k) record. The listed applicant is Site Microsurgical Systems, Inc.. It received FDA 510(k) clearance on 1988-09-12 under 510(k) number K883575. The device is classified under product code HMG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 30 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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