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FDA 510(k)

SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050

K-Number: K002468 · 2001-03-02

ApplicantSan UP S.A.
Decision Date2001-03-02
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050 is the device name listed in this FDA 510(k) record. The listed applicant is San UP S.A.. It received FDA 510(k) clearance on 2001-03-02 under 510(k) number K002468. 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 SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050?

SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050 is a medical device that received FDA 510(k) clearance on 2001-03-02. The listed applicant is San UP S.A.. The 510(k) number is K002468.

When did SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050 receive FDA 510(k) clearance?

SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050 received FDA 510(k) clearance on 2001-03-02, under 510(k) number K002468.

Who is the listed applicant for SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050?

The FDA 510(k) record lists San UP S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050?

The FDA product code for SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050 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.

Other records listing San UP S.A. 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.

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.

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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