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FDA 510(k)

OLYMPUS SD SERIES SNARES

K-Number: K955650 · 1996-03-29

ApplicantOlympus America, Inc.
Decision Date1996-03-29
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS SD SERIES SNARES is the device name listed in this FDA 510(k) record. The listed applicant is Olympus America, Inc.. It received FDA 510(k) clearance on 1996-03-29 under 510(k) number K955650. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS SD SERIES SNARES?

OLYMPUS SD SERIES SNARES is a medical device that received FDA 510(k) clearance on 1996-03-29. The listed applicant is Olympus America, Inc.. The 510(k) number is K955650.

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

OLYMPUS SD SERIES SNARES received FDA 510(k) clearance on 1996-03-29, under 510(k) number K955650.

Who is the listed applicant for OLYMPUS SD SERIES SNARES?

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

What is the FDA product code for OLYMPUS SD SERIES SNARES?

The FDA product code for OLYMPUS SD SERIES SNARES is FDI.

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Other records listing Olympus America, Inc. as applicant

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Related Devices (Code: FDI)

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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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