FDA 510(k)

CORDIS INFLATOR DEVICE

K-Number: K912644 · 1991-09-16

Decision Date1991-09-16

Product CodeMAV

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORDIS INFLATOR DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1991-09-16 under 510(k) number K912644. 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 CORDIS INFLATOR DEVICE?

CORDIS INFLATOR DEVICE is a medical device that received FDA 510(k) clearance on 1991-09-16. The listed applicant is Cordis Corp.. The 510(k) number is K912644.

When did CORDIS INFLATOR DEVICE receive FDA 510(k) clearance?

CORDIS INFLATOR DEVICE received FDA 510(k) clearance on 1991-09-16, under 510(k) number K912644.

Who is the listed applicant for CORDIS INFLATOR DEVICE?

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

What is the FDA product code for CORDIS INFLATOR DEVICE?

The FDA product code for CORDIS INFLATOR DEVICE is MAV.

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Related Devices (Code: MAV)

K260035Digital Indeflator INFLANTEUAB Telemedicina K220773Everest 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 Vascular K162272Fluent 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.