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FDA 510(k)

DISPOSABLE SLIDE VALVE MANIFOLD

K-Number: K913094 · 1992-01-27

ApplicantProfessional Medical Services
Decision Date1992-01-27
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SLIDE VALVE MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is Professional Medical Services. It received FDA 510(k) clearance on 1992-01-27 under 510(k) number K913094. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE SLIDE VALVE MANIFOLD?

DISPOSABLE SLIDE VALVE MANIFOLD is a medical device that received FDA 510(k) clearance on 1992-01-27. The listed applicant is Professional Medical Services. The 510(k) number is K913094.

When did DISPOSABLE SLIDE VALVE MANIFOLD receive FDA 510(k) clearance?

DISPOSABLE SLIDE VALVE MANIFOLD received FDA 510(k) clearance on 1992-01-27, under 510(k) number K913094.

Who is the listed applicant for DISPOSABLE SLIDE VALVE MANIFOLD?

The FDA 510(k) record lists Professional Medical Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE SLIDE VALVE MANIFOLD?

The FDA product code for DISPOSABLE SLIDE VALVE MANIFOLD is DQO.

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Other records listing Professional Medical Services as applicant

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K910378PRESSURE MONITORING EXTENSION LINEK904508CONDOR ANALOG INFLATION SYRINGEK904954CONDOR DIGITAL INFLATION SYRINGEK902606RADIOPAQUE RULERK884577PROCEDURE READY TRAYSK890471PMS ANGIO DRAPE

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Related Devices (Code: DQO)

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.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

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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