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FDA 510(k)

CORDIS CSF RESERVOIR

K-Number: K950315 · 1995-05-09

ApplicantCordis Corp.
Decision Date1995-05-09
Product CodeLKG
Advisory CommitteeNE
DecisionUnknown

Device Summary

CORDIS CSF RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1995-05-09 under 510(k) number K950315. The device is classified under product code LKG. It was reviewed by the NE advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CORDIS CSF RESERVOIR?

CORDIS CSF RESERVOIR is a medical device that received FDA 510(k) clearance on 1995-05-09. The listed applicant is Cordis Corp.. The 510(k) number is K950315.

When did CORDIS CSF RESERVOIR receive FDA 510(k) clearance?

CORDIS CSF RESERVOIR received FDA 510(k) clearance on 1995-05-09, under 510(k) number K950315.

Who is the listed applicant for CORDIS CSF RESERVOIR?

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 CSF RESERVOIR?

The FDA product code for CORDIS CSF RESERVOIR is LKG.

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Other records listing Cordis Corp. as applicant

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Related Devices (Code: LKG)

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.

K881690PORT-A-CATH PORTAL INTRODUCER FORCEPSPharmacia Deltec, Inc.K881493PORT-A-CATH IMPLANTABLE ACCESS SYSTEM - KIT CONF.Pharmacia Deltec, Inc.K874468P-S MEDICAL VENTRICULAR ACCESS PORTPudenz-Schulte Medical Research Corp.K874498CSF-VENTRICULOSTOMY RESERVOIRPudenz-Schulte Medical Research Corp.K833822P-S MEDICAL CSF ACCESS DEV 15MM/25MMPudenz-Schulte Medical Research Corp.K833672HH SUBCUTANEOUS ACCESS PORTHolter-Hausner Intl.

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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