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FDA 510(k)

HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM

K-Number: K891456 · 1989-06-23

ApplicantBaxter Healthcare Corp
Decision Date1989-06-23
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1989-06-23 under 510(k) number K891456. 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 HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM?

HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K891456.

When did HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM receive FDA 510(k) clearance?

HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM received FDA 510(k) clearance on 1989-06-23, under 510(k) number K891456.

Who is the listed applicant for HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM?

The FDA product code for HEYER-SCHULTE (CSF) VENTRI ACCESS(RESERV/ANTECHAM 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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