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FDA 510(k)

SILENTFLOW 2 EXHALATION SYSTEM, MODEL WM 23650

K-Number: K022934 · 2002-11-14

ApplicantGottlieb Weinmann Geraete Fuer Medizin Und Arbeits
Decision Date2002-11-14
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SILENTFLOW 2 EXHALATION SYSTEM, MODEL WM 23650 is the device name listed in this FDA 510(k) record. The listed applicant is Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits. It received FDA 510(k) clearance on 2002-11-14 under 510(k) number K022934. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILENTFLOW 2 EXHALATION SYSTEM, MODEL WM 23650?

SILENTFLOW 2 EXHALATION SYSTEM, MODEL WM 23650 is a medical device that received FDA 510(k) clearance on 2002-11-14. The listed applicant is Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits. The 510(k) number is K022934.

When did SILENTFLOW 2 EXHALATION SYSTEM, MODEL WM 23650 receive FDA 510(k) clearance?

SILENTFLOW 2 EXHALATION SYSTEM, MODEL WM 23650 received FDA 510(k) clearance on 2002-11-14, under 510(k) number K022934.

Who is the listed applicant for SILENTFLOW 2 EXHALATION SYSTEM, MODEL WM 23650?

The FDA 510(k) record lists Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILENTFLOW 2 EXHALATION SYSTEM, MODEL WM 23650?

The FDA product code for SILENTFLOW 2 EXHALATION SYSTEM, MODEL WM 23650 is BZD.

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Other records listing Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits 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.

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Official Source

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