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FDA 510(k)

MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER

K-Number: K041974 · 2004-08-24

ApplicantMed2000 S.R.L.
Decision Date2004-08-24
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Med2000 S.R.L.. It received FDA 510(k) clearance on 2004-08-24 under 510(k) number K041974. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER?

MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER is a medical device that received FDA 510(k) clearance on 2004-08-24. The listed applicant is Med2000 S.R.L.. The 510(k) number is K041974.

When did MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER receive FDA 510(k) clearance?

MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER received FDA 510(k) clearance on 2004-08-24, under 510(k) number K041974.

Who is the listed applicant for MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER?

The FDA 510(k) record lists Med2000 S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER?

The FDA product code for MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER is BTI.

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 Med2000 S.R.L. 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.

K041327MED2000 SPA NEBULIZER ANDYFLOW, MODEL A1/C WITH ACCESSORIESK031908MED2000 SPA NEBULIZER COMPRESSORS, MODELS P1 AND P2, WITH NEBULIZER, AND MED2000 SPA NEBULIZER, MODEL A1/C (ANDYFLOW)

Related Devices (Code: BTI)

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.

K131881OMBRA TABLE TOP COMPRESSORTrudell Medical Intl.K113338MEDICAL AIR COMPRESSOROricare, Inc.K091871DK50 DSEkom S.R.O.K072634EMG TRITON -COMP,MODEL NCA01-XXX SERIESEmg Technology Co., Ltd.K060781MEDICAL COMPRESSOR, MODELS DK50 D AND DMEkom S.R.O.K051691MINIMATE COMPRESSORPrecision Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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