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FDA 510(k)

SD SNARES

K-Number: K902735 · 1990-08-02

ApplicantOlympus Corp.
Decision Date1990-08-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SD SNARES is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1990-08-02 under 510(k) number K902735. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SD SNARES?

SD SNARES is a medical device that received FDA 510(k) clearance on 1990-08-02. The listed applicant is Olympus Corp.. The 510(k) number is K902735.

When did SD SNARES receive FDA 510(k) clearance?

SD SNARES received FDA 510(k) clearance on 1990-08-02, under 510(k) number K902735.

Who is the listed applicant for SD SNARES?

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

What is the FDA product code for SD SNARES?

The FDA product code for SD SNARES is GEI.

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Other records listing Olympus Corp. as applicant

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Related Devices (Code: GEI)

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.

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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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