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FDA 510(k)

BAXTER SINGLE PATIENT USE PRESSURE INFUSOR

K-Number: K904484 · 1990-10-26

ApplicantTecnadyne Scientific, Inc.
Decision Date1990-10-26
Product CodeKZD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BAXTER SINGLE PATIENT USE PRESSURE INFUSOR is the device name listed in this FDA 510(k) record. The listed applicant is Tecnadyne Scientific, Inc.. It received FDA 510(k) clearance on 1990-10-26 under 510(k) number K904484. 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 BAXTER SINGLE PATIENT USE PRESSURE INFUSOR?

BAXTER SINGLE PATIENT USE PRESSURE INFUSOR is a medical device that received FDA 510(k) clearance on 1990-10-26. The listed applicant is Tecnadyne Scientific, Inc.. The 510(k) number is K904484.

When did BAXTER SINGLE PATIENT USE PRESSURE INFUSOR receive FDA 510(k) clearance?

BAXTER SINGLE PATIENT USE PRESSURE INFUSOR received FDA 510(k) clearance on 1990-10-26, under 510(k) number K904484.

Who is the listed applicant for BAXTER SINGLE PATIENT USE PRESSURE INFUSOR?

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

What is the FDA product code for BAXTER SINGLE PATIENT USE PRESSURE INFUSOR?

The FDA product code for BAXTER SINGLE PATIENT USE PRESSURE INFUSOR is KZD.

Related Clinical Trials

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.

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Other records listing Tecnadyne Scientific, Inc. as applicant

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.

K940431TECNADYNE 20/20 FOG INHIBITOR KITK940891TECNADYNE ENDOSCOPIC INSTRUMENT HOLDERK910926TECNADYNE SURGI-SQUEEZE INFUSION PUMPK912007BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF

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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