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FDA 510(k)

PRESSURE INFUSER

K-Number: K820159 · 1982-04-21

ApplicantDavid Clark Company, Inc.
Decision Date1982-04-21
Product CodeKZD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRESSURE INFUSER is the device name listed in this FDA 510(k) record. The listed applicant is David Clark Company, Inc.. It received FDA 510(k) clearance on 1982-04-21 under 510(k) number K820159. 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 PRESSURE INFUSER?

PRESSURE INFUSER is a medical device that received FDA 510(k) clearance on 1982-04-21. The listed applicant is David Clark Company, Inc.. The 510(k) number is K820159.

When did PRESSURE INFUSER receive FDA 510(k) clearance?

PRESSURE INFUSER received FDA 510(k) clearance on 1982-04-21, under 510(k) number K820159.

Who is the listed applicant for PRESSURE INFUSER?

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

What is the FDA product code for PRESSURE INFUSER?

The FDA product code for PRESSURE INFUSER is KZD.

Related Clinical Trials

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Related Devices (Code: KZD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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

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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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