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FDA 510(k)

MX820-5 PRESSURE INFUSOR 500CC MX820-10

K-Number: K800560 · 1980-04-29

ApplicantMedex, Inc.
Decision Date1980-04-29
Product CodeKZD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MX820-5 PRESSURE INFUSOR 500CC MX820-10 is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1980-04-29 under 510(k) number K800560. The device is classified under product code KZD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MX820-5 PRESSURE INFUSOR 500CC MX820-10?

MX820-5 PRESSURE INFUSOR 500CC MX820-10 is a medical device that received FDA 510(k) clearance on 1980-04-29. The listed applicant is Medex, Inc.. The 510(k) number is K800560.

When did MX820-5 PRESSURE INFUSOR 500CC MX820-10 receive FDA 510(k) clearance?

MX820-5 PRESSURE INFUSOR 500CC MX820-10 received FDA 510(k) clearance on 1980-04-29, under 510(k) number K800560.

Who is the listed applicant for MX820-5 PRESSURE INFUSOR 500CC MX820-10?

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

What is the FDA product code for MX820-5 PRESSURE INFUSOR 500CC MX820-10?

The FDA product code for MX820-5 PRESSURE INFUSOR 500CC MX820-10 is KZD.

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Related Devices (Code: KZD)

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K974074INFUSION DYNAMICS POWER INFUSERInfusion Dynamics, Inc.K973843MSI PRESSURE INFUSORSmith Assoc.K953290OLYMPUS AUTOMATIC SURGICAL IRRIGATION PUMPOlympus America, Inc.K951988PRESSURIZERPromedic, Inc.K942933PRESSURE INFUSION CUFFCirculatory Technology, Inc.K930012KAWASUMI LABORATORIES K-CUFFKawasumi Laboratories Co., Ltd.

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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