Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LMT-KATH-S; LMT-KATH-I

K-Number: K062308 · 2007-03-20

ApplicantLicher Medizintechnologie GmbH
Decision Date2007-03-20
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LMT-KATH-S; LMT-KATH-I is the device name listed in this FDA 510(k) record. The listed applicant is Licher Medizintechnologie GmbH. It received FDA 510(k) clearance on 2007-03-20 under 510(k) number K062308. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LMT-KATH-S; LMT-KATH-I?

LMT-KATH-S; LMT-KATH-I is a medical device that received FDA 510(k) clearance on 2007-03-20. The listed applicant is Licher Medizintechnologie GmbH. The 510(k) number is K062308.

When did LMT-KATH-S; LMT-KATH-I receive FDA 510(k) clearance?

LMT-KATH-S; LMT-KATH-I received FDA 510(k) clearance on 2007-03-20, under 510(k) number K062308.

Who is the listed applicant for LMT-KATH-S; LMT-KATH-I?

The FDA 510(k) record lists Licher Medizintechnologie GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LMT-KATH-S; LMT-KATH-I?

The FDA product code for LMT-KATH-S; LMT-KATH-I is FPA.

Related Devices (Code: FPA)

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

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.

↑