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FDA 510(k)

OLYMPUS 5FR SEMI-RIGID SCISSORS FOR OB/GYN

K-Number: K950036 · 1995-02-09

ApplicantOlympus America, Inc.
Decision Date1995-02-09
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OLYMPUS 5FR SEMI-RIGID SCISSORS FOR OB/GYN 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 1995-02-09 under 510(k) number K950036. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS 5FR SEMI-RIGID SCISSORS FOR OB/GYN?

OLYMPUS 5FR SEMI-RIGID SCISSORS FOR OB/GYN is a medical device that received FDA 510(k) clearance on 1995-02-09. The listed applicant is Olympus America, Inc.. The 510(k) number is K950036.

When did OLYMPUS 5FR SEMI-RIGID SCISSORS FOR OB/GYN receive FDA 510(k) clearance?

OLYMPUS 5FR SEMI-RIGID SCISSORS FOR OB/GYN received FDA 510(k) clearance on 1995-02-09, under 510(k) number K950036.

Who is the listed applicant for OLYMPUS 5FR SEMI-RIGID SCISSORS FOR OB/GYN?

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 5FR SEMI-RIGID SCISSORS FOR OB/GYN?

The FDA product code for OLYMPUS 5FR SEMI-RIGID SCISSORS FOR OB/GYN is HIH.

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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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