FDA 510(k)

SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT

K-Number: K962931 · 1996-10-21

ApplicantSmiths Industries Medical Systems, Inc.

Decision Date1996-10-21

Product CodeJKA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Smiths Industries Medical Systems, Inc.. It received FDA 510(k) clearance on 1996-10-21 under 510(k) number K962931. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT?

SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT is a medical device that received FDA 510(k) clearance on 1996-10-21. The listed applicant is Smiths Industries Medical Systems, Inc.. The 510(k) number is K962931.

When did SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT receive FDA 510(k) clearance?

SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT received FDA 510(k) clearance on 1996-10-21, under 510(k) number K962931.

Who is the listed applicant for SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT?

The FDA 510(k) record lists Smiths Industries Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT?

The FDA product code for SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT is JKA.

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Other records listing Smiths Industries Medical Systems, 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.