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FDA 510(k)

PRESSURIZER

K-Number: K951988 · 1995-06-14

ApplicantPromedic, Inc.
Decision Date1995-06-14
Product CodeKZD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRESSURIZER is the device name listed in this FDA 510(k) record. The listed applicant is Promedic, Inc.. It received FDA 510(k) clearance on 1995-06-14 under 510(k) number K951988. 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 PRESSURIZER?

PRESSURIZER is a medical device that received FDA 510(k) clearance on 1995-06-14. The listed applicant is Promedic, Inc.. The 510(k) number is K951988.

When did PRESSURIZER receive FDA 510(k) clearance?

PRESSURIZER received FDA 510(k) clearance on 1995-06-14, under 510(k) number K951988.

Who is the listed applicant for PRESSURIZER?

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

What is the FDA product code for PRESSURIZER?

The FDA product code for PRESSURIZER is KZD.

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Other records listing Promedic, 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.

K112318CLEARPATH 24K072756NON-IV ADAPTER FOR INFANT NG TUBEK060497BABYAIRK060842REVJET TURBOK052903PEDIATRIC FEEDING TUBEK031409URINARY CATHETERS

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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.K942933PRESSURE INFUSION CUFFCirculatory Technology, Inc.K930012KAWASUMI LABORATORIES K-CUFFKawasumi Laboratories Co., Ltd.K921168ALLEN INFUSION PUMP MODEL 3000 AND IRRIGATION 2000Allen Medical Systems, Inc.

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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