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FDA 510(k)

MEDCOMP'S FEMORAL VEIN CATHETERS

K-Number: K860810 · 1986-04-08

ApplicantMedical Components, Inc.
Decision Date1986-04-08
Product CodeLFK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDCOMP'S FEMORAL VEIN CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1986-04-08 under 510(k) number K860810. The device is classified under product code LFK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCOMP'S FEMORAL VEIN CATHETERS?

MEDCOMP'S FEMORAL VEIN CATHETERS is a medical device that received FDA 510(k) clearance on 1986-04-08. The listed applicant is Medical Components, Inc.. The 510(k) number is K860810.

When did MEDCOMP'S FEMORAL VEIN CATHETERS receive FDA 510(k) clearance?

MEDCOMP'S FEMORAL VEIN CATHETERS received FDA 510(k) clearance on 1986-04-08, under 510(k) number K860810.

Who is the listed applicant for MEDCOMP'S FEMORAL VEIN CATHETERS?

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

What is the FDA product code for MEDCOMP'S FEMORAL VEIN CATHETERS?

The FDA product code for MEDCOMP'S FEMORAL VEIN CATHETERS is LFK.

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Other records listing Medical Components, 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.

K25083614F Duo-Flow® Side X Side Double Lumen CatheterK1316876F X 60CM TRIPLE PRO-LINE CT BASIC IR SETK1306872F & 3F VASCU-SHEATH TEARAWAY INTRODUCERK1309235F DIGNITY CT TITANIUM PORTK124046VALVED TEARAWAY INTRODUCER GENERATION IIK1236173F PRO-PICC

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Related Devices (Code: LFK)

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.

K971897CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH)Medron, Inc.K914936CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SETAkcess Medical Products, Inc.K915215CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITSAkcess Medical Products, Inc.K891763FC-100 FEMORAL CATHETERAkcess Medical Products, Inc.K891764FC-101 FEMORAL CATHETER GUIDE WIREAkcess Medical Products, Inc.K890717MODIFICATION HEMOFILTRATION CATHETER HF-100Vas-Cath, 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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