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FDA 510(k)

AESCULAP VENTRICULOSCOPE SYSTEM

K-Number: K954394 · 1996-03-07

ApplicantAesculap, Inc.
Decision Date1996-03-07
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AESCULAP VENTRICULOSCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1996-03-07 under 510(k) number K954394. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP VENTRICULOSCOPE SYSTEM?

AESCULAP VENTRICULOSCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 1996-03-07. The listed applicant is Aesculap, Inc.. The 510(k) number is K954394.

When did AESCULAP VENTRICULOSCOPE SYSTEM receive FDA 510(k) clearance?

AESCULAP VENTRICULOSCOPE SYSTEM received FDA 510(k) clearance on 1996-03-07, under 510(k) number K954394.

Who is the listed applicant for AESCULAP VENTRICULOSCOPE SYSTEM?

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

What is the FDA product code for AESCULAP VENTRICULOSCOPE SYSTEM?

The FDA product code for AESCULAP VENTRICULOSCOPE SYSTEM is GWG.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: GWG)

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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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