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FDA 510(k)

BIOCUFF INFUSION BAG PRESSOR

K-Number: K832377 · 1983-08-12

ApplicantBio-Medical Instruments , Ltd.
Decision Date1983-08-12
Product CodeKZD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BIOCUFF INFUSION BAG PRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Medical Instruments , Ltd.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832377. 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 BIOCUFF INFUSION BAG PRESSOR?

BIOCUFF INFUSION BAG PRESSOR is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Bio-Medical Instruments , Ltd.. The 510(k) number is K832377.

When did BIOCUFF INFUSION BAG PRESSOR receive FDA 510(k) clearance?

BIOCUFF INFUSION BAG PRESSOR received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832377.

Who is the listed applicant for BIOCUFF INFUSION BAG PRESSOR?

The FDA 510(k) record lists Bio-Medical Instruments , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOCUFF INFUSION BAG PRESSOR?

The FDA product code for BIOCUFF INFUSION BAG PRESSOR is KZD.

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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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