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FDA 510(k)

AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV

K-Number: K030698 · 2003-03-20

ApplicantAesculap, Inc.
Decision Date2003-03-20
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2003-03-20 under 510(k) number K030698. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV?

AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV is a medical device that received FDA 510(k) clearance on 2003-03-20. The listed applicant is Aesculap, Inc.. The 510(k) number is K030698.

When did AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV receive FDA 510(k) clearance?

AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV received FDA 510(k) clearance on 2003-03-20, under 510(k) number K030698.

Who is the listed applicant for AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV?

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 - MIETHKE SHUNT SYSTEM W/ NPH-DSV?

The FDA product code for AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV is JXG.

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Related Devices (Code: JXG)

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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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