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FDA 510(k)

MIETHKE SHUNT SYSTEM

K-Number: K020728 · 2002-04-05

ApplicantAesculap, Inc.
Decision Date2002-04-05
Product CodeHCA
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MIETHKE SHUNT 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 2002-04-05 under 510(k) number K020728. The device is classified under product code HCA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIETHKE SHUNT SYSTEM?

MIETHKE SHUNT SYSTEM is a medical device that received FDA 510(k) clearance on 2002-04-05. The listed applicant is Aesculap, Inc.. The 510(k) number is K020728.

When did MIETHKE SHUNT SYSTEM receive FDA 510(k) clearance?

MIETHKE SHUNT SYSTEM received FDA 510(k) clearance on 2002-04-05, under 510(k) number K020728.

Who is the listed applicant for MIETHKE SHUNT 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 MIETHKE SHUNT SYSTEM?

The FDA product code for MIETHKE SHUNT SYSTEM is HCA.

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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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