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FDA 510(k)

CENTRAL VENOUS PRESSURE MANOMETER

K-Number: K904674 · 1990-12-27

ApplicantMedex, Inc.
Decision Date1990-12-27
Product CodeKRK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL VENOUS PRESSURE MANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1990-12-27 under 510(k) number K904674. The device is classified under product code KRK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRAL VENOUS PRESSURE MANOMETER?

CENTRAL VENOUS PRESSURE MANOMETER is a medical device that received FDA 510(k) clearance on 1990-12-27. The listed applicant is Medex, Inc.. The 510(k) number is K904674.

When did CENTRAL VENOUS PRESSURE MANOMETER receive FDA 510(k) clearance?

CENTRAL VENOUS PRESSURE MANOMETER received FDA 510(k) clearance on 1990-12-27, under 510(k) number K904674.

Who is the listed applicant for CENTRAL VENOUS PRESSURE MANOMETER?

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 CENTRAL VENOUS PRESSURE MANOMETER?

The FDA product code for CENTRAL VENOUS PRESSURE MANOMETER is KRK.

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Other records listing Medex, 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.

K042432PHARMGUARD TOOLBOX, MODEL G6000782K040899MEDEX 3000 SERIES MR SYRINGE INFUSION PUMPK020780TRANSTAR INTRACRANIAL PRESSURE TRANSDUCER, MODEL MX950ICPK000328MEDEX 3000 SERIES MRI COMPATIBLE SYRINGE INFUSION PUMPK982640MEDEX 3000 SERIES SYRINGE INFUSION PUMPK982123CONTRAST CONTROL DEVICE

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Related Devices (Code: KRK)

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.

K950607UST-5268P-5 TRANSDUCERAloka Co., Ltd.K884386ADMINISTRATION/MANOMETER SET W/3 WAY STOPCOCKEthitek Pharmaceuticals Co.K875322MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETERSchneider-Shilley (Usa)K861605SCHNEIDER-SHILEY PRESSURE MANOMETERShiley, Inc.K830910MANOMETER SET C.V.P. #S 298/299Exco, Inc.K813498MEDIFIXBurron Medical Products, 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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