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FDA 510(k)

MODEL AR-6300 INFUSION PUMP

K-Number: K915721 · 1992-03-19

ApplicantArthrex, Inc.
Decision Date1992-03-19
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODEL AR-6300 INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 1992-03-19 under 510(k) number K915721. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL AR-6300 INFUSION PUMP?

MODEL AR-6300 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1992-03-19. The listed applicant is Arthrex, Inc.. The 510(k) number is K915721.

When did MODEL AR-6300 INFUSION PUMP receive FDA 510(k) clearance?

MODEL AR-6300 INFUSION PUMP received FDA 510(k) clearance on 1992-03-19, under 510(k) number K915721.

Who is the listed applicant for MODEL AR-6300 INFUSION PUMP?

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

What is the FDA product code for MODEL AR-6300 INFUSION PUMP?

The FDA product code for MODEL AR-6300 INFUSION PUMP is HRX.

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Related Devices (Code: HRX)

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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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