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FDA 510(k)

PARKER AMBULATORY MEDICATION INFUSION PUMP 2004

K-Number: K897086 · 1990-09-28

ApplicantParker Hannifin Corp.
Decision Date1990-09-28
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PARKER AMBULATORY MEDICATION INFUSION PUMP 2004 is the device name listed in this FDA 510(k) record. The listed applicant is Parker Hannifin Corp.. It received FDA 510(k) clearance on 1990-09-28 under 510(k) number K897086. 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 PARKER AMBULATORY MEDICATION INFUSION PUMP 2004?

PARKER AMBULATORY MEDICATION INFUSION PUMP 2004 is a medical device that received FDA 510(k) clearance on 1990-09-28. The listed applicant is Parker Hannifin Corp.. The 510(k) number is K897086.

When did PARKER AMBULATORY MEDICATION INFUSION PUMP 2004 receive FDA 510(k) clearance?

PARKER AMBULATORY MEDICATION INFUSION PUMP 2004 received FDA 510(k) clearance on 1990-09-28, under 510(k) number K897086.

Who is the listed applicant for PARKER AMBULATORY MEDICATION INFUSION PUMP 2004?

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

What is the FDA product code for PARKER AMBULATORY MEDICATION INFUSION PUMP 2004?

The FDA product code for PARKER AMBULATORY MEDICATION INFUSION PUMP 2004 is FRN.

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Other records listing Parker Hannifin Corp. as applicant

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Related Devices (Code: FRN)

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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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