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FDA 510(k)

MEDCOMP VASCU-PICC & MIDLINE CATHETERS

K-Number: K121094 · 2012-06-06

Decision Date2012-06-06
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDCOMP VASCU-PICC & MIDLINE 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 2012-06-06 under 510(k) number K121094. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCOMP VASCU-PICC & MIDLINE CATHETERS?

MEDCOMP VASCU-PICC & MIDLINE CATHETERS is a medical device that received FDA 510(k) clearance on 2012-06-06. The listed applicant is Medical Components, Inc.. The 510(k) number is K121094.

When did MEDCOMP VASCU-PICC & MIDLINE CATHETERS receive FDA 510(k) clearance?

MEDCOMP VASCU-PICC & MIDLINE CATHETERS received FDA 510(k) clearance on 2012-06-06, under 510(k) number K121094.

Who is the listed applicant for MEDCOMP VASCU-PICC & MIDLINE 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 VASCU-PICC & MIDLINE CATHETERS?

The FDA product code for MEDCOMP VASCU-PICC & MIDLINE CATHETERS is LJS.

Related Clinical Trials

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.

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.

View all 61 devices →

Related Devices (Code: LJS)

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.

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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