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FDA 510(k)

PORT-A-CATH PORTAL INTRODUCER FORCEPS

K-Number: K881690 · 1988-05-20

ApplicantPharmacia Deltec, Inc.
Decision Date1988-05-20
Product CodeLKG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PORT-A-CATH PORTAL INTRODUCER FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Deltec, Inc.. It received FDA 510(k) clearance on 1988-05-20 under 510(k) number K881690. The device is classified under product code LKG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORT-A-CATH PORTAL INTRODUCER FORCEPS?

PORT-A-CATH PORTAL INTRODUCER FORCEPS is a medical device that received FDA 510(k) clearance on 1988-05-20. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K881690.

When did PORT-A-CATH PORTAL INTRODUCER FORCEPS receive FDA 510(k) clearance?

PORT-A-CATH PORTAL INTRODUCER FORCEPS received FDA 510(k) clearance on 1988-05-20, under 510(k) number K881690.

Who is the listed applicant for PORT-A-CATH PORTAL INTRODUCER FORCEPS?

The FDA 510(k) record lists Pharmacia Deltec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORT-A-CATH PORTAL INTRODUCER FORCEPS?

The FDA product code for PORT-A-CATH PORTAL INTRODUCER FORCEPS is LKG.

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Other records listing Pharmacia Deltec, 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.

K943310MODEL 6100 AMBULATORY INFUSION SYSTEMK942046PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVEK942161LOCKBOXK942024PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEMK941445EXTENSION SET WITH ANTI-SIPHON VALVEK931073CATH-FINDER

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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.

K950315CORDIS CSF RESERVOIRCordis Corp.K881493PORT-A-CATH IMPLANTABLE ACCESS SYSTEM - KIT CONF.Pharmacia Deltec, Inc.K874498CSF-VENTRICULOSTOMY RESERVOIRPudenz-Schulte Medical Research Corp.K874468P-S MEDICAL VENTRICULAR ACCESS PORTPudenz-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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