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FDA 510(k)

SIMS PORTEX ANESTHESIA CATHETER

K-Number: K994275 · 2000-02-22

ApplicantSims Portex, Inc.
Decision Date2000-02-22
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SIMS PORTEX ANESTHESIA CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Sims Portex, Inc.. It received FDA 510(k) clearance on 2000-02-22 under 510(k) number K994275. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMS PORTEX ANESTHESIA CATHETER?

SIMS PORTEX ANESTHESIA CATHETER is a medical device that received FDA 510(k) clearance on 2000-02-22. The listed applicant is Sims Portex, Inc.. The 510(k) number is K994275.

When did SIMS PORTEX ANESTHESIA CATHETER receive FDA 510(k) clearance?

SIMS PORTEX ANESTHESIA CATHETER received FDA 510(k) clearance on 2000-02-22, under 510(k) number K994275.

Who is the listed applicant for SIMS PORTEX ANESTHESIA CATHETER?

The FDA 510(k) record lists Sims Portex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIMS PORTEX ANESTHESIA CATHETER?

The FDA product code for SIMS PORTEX ANESTHESIA CATHETER is FRN.

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Other records listing Sims Portex, Inc. as applicant

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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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