PORT-A-CATH PORTAL INTRODUCER FORCEPS— 510(k) K881690

Name: FDA 510(k) clearance K881690
Creator: U.S. Food and Drug Administration
Published: 1988-05-20

Substantially Equivalent

Pharmacia Deltec, Inc.

FDA 510(k) clearance K881690 for PORT-A-CATH PORTAL INTRODUCER FORCEPS, Substantially Equivalent on 1988-05-20. Applicant: Pharmacia Deltec, Inc.. Device class: 2.

Clearance details

Applicant: Pharmacia Deltec, Inc.
Product code: Code LKG
Device class: Class 2
Regulation: 21 CFR 882.5550
Advisory panel: Neurology
Date received: 1988-04-19
Decision date: 1988-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LKG

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K950315 — CORDIS CSF RESERVOIR1995-05-09
K881493 — PORT-A-CATH IMPLANTABLE ACCESS SYSTEM - KIT CONF.1988-05-20
K874468 — P-S MEDICAL VENTRICULAR ACCESS PORT1988-02-11
K874498 — CSF-VENTRICULOSTOMY RESERVOIR1988-02-11
K833822 — P-S MEDICAL CSF ACCESS DEV 15MM/25MM1984-05-25

More clearances from Pharmacia Deltec, Inc.

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K943310 — MODEL 6100 AMBULATORY INFUSION SYSTEM1995-02-21
K942046 — PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE1994-10-04
K942161 — LOCKBOX1994-08-02
K942024 — PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEM1994-07-26
K941445 — EXTENSION SET WITH ANTI-SIPHON VALVE1994-06-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.