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FDA 510(k)

STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT

K-Number: K003577 · 2001-01-29

ApplicantSTERIS Corporation
Decision Date2001-01-29
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2001-01-29 under 510(k) number K003577. The device is classified under product code FST. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT?

STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT is a medical device that received FDA 510(k) clearance on 2001-01-29. The listed applicant is STERIS Corporation. The 510(k) number is K003577.

When did STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT receive FDA 510(k) clearance?

STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT received FDA 510(k) clearance on 2001-01-29, under 510(k) number K003577.

Who is the listed applicant for STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT?

The FDA 510(k) record lists STERIS Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT?

The FDA product code for STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT is FST.

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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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