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FDA 510(k)

RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER

K-Number: K882975 · 1989-01-25

ApplicantRichmann Laboratories
Decision Date1989-01-25
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER is the device name listed in this FDA 510(k) record. The listed applicant is Richmann Laboratories. It received FDA 510(k) clearance on 1989-01-25 under 510(k) number K882975. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER?

RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER is a medical device that received FDA 510(k) clearance on 1989-01-25. The listed applicant is Richmann Laboratories. The 510(k) number is K882975.

When did RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER receive FDA 510(k) clearance?

RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER received FDA 510(k) clearance on 1989-01-25, under 510(k) number K882975.

Who is the listed applicant for RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER?

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

What is the FDA product code for RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER?

The FDA product code for RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER is FMF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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