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FDA 510(k)

SURGICAL LIGHTING-CENTRA 450

K-Number: K902864 · 1990-09-10

Decision Date1990-09-10
Product CodeFSY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL LIGHTING-CENTRA 450 is the device name listed in this FDA 510(k) record. The listed applicant is Sds Dental, Inc.. It received FDA 510(k) clearance on 1990-09-10 under 510(k) number K902864. The device is classified under product code FSY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL LIGHTING-CENTRA 450?

SURGICAL LIGHTING-CENTRA 450 is a medical device that received FDA 510(k) clearance on 1990-09-10. The listed applicant is Sds Dental, Inc.. The 510(k) number is K902864.

When did SURGICAL LIGHTING-CENTRA 450 receive FDA 510(k) clearance?

SURGICAL LIGHTING-CENTRA 450 received FDA 510(k) clearance on 1990-09-10, under 510(k) number K902864.

Who is the listed applicant for SURGICAL LIGHTING-CENTRA 450?

The FDA 510(k) record lists Sds Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL LIGHTING-CENTRA 450?

The FDA product code for SURGICAL LIGHTING-CENTRA 450 is FSY.

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 Sds Dental, 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 21 devices →

Related Devices (Code: FSY)

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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