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FDA 510(k)

COLUMBUS (PS)

K-Number: K030367 · 2003-08-21

ApplicantAesculap, Inc.
Decision Date2003-08-21
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COLUMBUS (PS) is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2003-08-21 under 510(k) number K030367. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLUMBUS (PS)?

COLUMBUS (PS) is a medical device that received FDA 510(k) clearance on 2003-08-21. The listed applicant is Aesculap, Inc.. The 510(k) number is K030367.

When did COLUMBUS (PS) receive FDA 510(k) clearance?

COLUMBUS (PS) received FDA 510(k) clearance on 2003-08-21, under 510(k) number K030367.

Who is the listed applicant for COLUMBUS (PS)?

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 COLUMBUS (PS)?

The FDA product code for COLUMBUS (PS) is JWH.

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Related Devices (Code: JWH)

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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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