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FDA 510(k)

REUSABLE STERILCONTAINER FILTER MODEL #JK090

K-Number: K041623 · 2004-12-13

ApplicantAesculap, Inc.
Decision Date2004-12-13
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

REUSABLE STERILCONTAINER FILTER MODEL #JK090 is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2004-12-13 under 510(k) number K041623. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSABLE STERILCONTAINER FILTER MODEL #JK090?

REUSABLE STERILCONTAINER FILTER MODEL #JK090 is a medical device that received FDA 510(k) clearance on 2004-12-13. The listed applicant is Aesculap, Inc.. The 510(k) number is K041623.

When did REUSABLE STERILCONTAINER FILTER MODEL #JK090 receive FDA 510(k) clearance?

REUSABLE STERILCONTAINER FILTER MODEL #JK090 received FDA 510(k) clearance on 2004-12-13, under 510(k) number K041623.

Who is the listed applicant for REUSABLE STERILCONTAINER FILTER MODEL #JK090?

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 REUSABLE STERILCONTAINER FILTER MODEL #JK090?

The FDA product code for REUSABLE STERILCONTAINER FILTER MODEL #JK090 is FRG.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: FRG)

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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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