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FDA 510(k)

CONDOR ANALOG INFLATION SYRINGE

K-Number: K904508 · 1991-04-02

ApplicantProfessional Medical Services
Decision Date1991-04-02
Product CodeMAV
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONDOR ANALOG INFLATION SYRINGE 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 1991-04-02 under 510(k) number K904508. The device is classified under product code MAV. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONDOR ANALOG INFLATION SYRINGE?

CONDOR ANALOG INFLATION SYRINGE is a medical device that received FDA 510(k) clearance on 1991-04-02. The listed applicant is Professional Medical Services. The 510(k) number is K904508.

When did CONDOR ANALOG INFLATION SYRINGE receive FDA 510(k) clearance?

CONDOR ANALOG INFLATION SYRINGE received FDA 510(k) clearance on 1991-04-02, under 510(k) number K904508.

Who is the listed applicant for CONDOR ANALOG INFLATION SYRINGE?

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 CONDOR ANALOG INFLATION SYRINGE?

The FDA product code for CONDOR ANALOG INFLATION SYRINGE is MAV.

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Other records listing Professional Medical Services 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.

K913094DISPOSABLE SLIDE VALVE MANIFOLDK910378PRESSURE MONITORING EXTENSION LINEK904954CONDOR DIGITAL INFLATION SYRINGEK902606RADIOPAQUE RULERK884577PROCEDURE READY TRAYSK890471PMS ANGIO DRAPE

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Related Devices (Code: MAV)

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.

K260035Digital Indeflator INFLANTEUAB TelemedicinaK220773Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)Medtronic VascularK162272Fluent inflation deviceVascular Solutions, Inc.K153038Everest 20 Disposable Inflation Device, Everest 20 Survival Kit, Everest 30 Disposable Inflation Device, Everest 30 Survival KitMedtronic, Inc.K153672basixTOUCH40 Inflation SyringeMerit Medical Systems, Inc.K130566BASIXTOUCHMerit 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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