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FDA 510(k)

LMT NOMAG IC 3.0

K-Number: K062052 · 2006-07-31

ApplicantLmt Lammers Medical Technology GmbH
Decision Date2006-07-31
Product CodeFPL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LMT NOMAG IC 3.0 is the device name listed in this FDA 510(k) record. The listed applicant is Lmt Lammers Medical Technology GmbH. It received FDA 510(k) clearance on 2006-07-31 under 510(k) number K062052. The device is classified under product code FPL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LMT NOMAG IC 3.0?

LMT NOMAG IC 3.0 is a medical device that received FDA 510(k) clearance on 2006-07-31. The listed applicant is Lmt Lammers Medical Technology GmbH. The 510(k) number is K062052.

When did LMT NOMAG IC 3.0 receive FDA 510(k) clearance?

LMT NOMAG IC 3.0 received FDA 510(k) clearance on 2006-07-31, under 510(k) number K062052.

Who is the listed applicant for LMT NOMAG IC 3.0?

The FDA 510(k) record lists Lmt Lammers Medical Technology GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LMT NOMAG IC 3.0?

The FDA product code for LMT NOMAG IC 3.0 is FPL.

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.

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Other records listing Lmt Lammers Medical Technology GmbH 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.

K033565LMT NOMAG IC 1,5

Related Devices (Code: FPL)

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.

K220742NxtGen Infant Transport IncubatorInternational BiomedicalK161918SREE MRI Transport IncubatorAdvanced Imaging Research Dba Sree Medical SystemsK123937ATOM TRANSCAPSULE V-707Atom Medical CorporationK103523185A+ TRANSPORT INCUBATOR WITH MASIMO PULSEOX, 185A+ TRANSPORT INCUBATOR WITH NELLCOR PULSEOXInternational Biomedical, Ltd.K103525A750I TRANSPORT INCUBATOR WITH MASIMO PLUSEOX, A750I TRANSPORT INCUBATOR WITH NELLOR PULSEOXInternational Biomedical, Ltd.K103524VOYAGER TRANSPORT INCUBATOR WITH MASIMO PULSEOX, VOYAGER TRANSPORT INCUBATOR WITH NELLCOR PULSEOXInternational Biomedical, Ltd.

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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