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FDA 510(k)

OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER

K-Number: K072418 · 2007-09-12

Decision Date2007-09-12
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER is the device name listed in this FDA 510(k) record. The listed applicant is Respironics New Jersey, Inc.. It received FDA 510(k) clearance on 2007-09-12 under 510(k) number K072418. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER?

OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER is a medical device that received FDA 510(k) clearance on 2007-09-12. The listed applicant is Respironics New Jersey, Inc.. The 510(k) number is K072418.

When did OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER receive FDA 510(k) clearance?

OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER received FDA 510(k) clearance on 2007-09-12, under 510(k) number K072418.

Who is the listed applicant for OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER?

The FDA 510(k) record lists Respironics New Jersey, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER?

The FDA product code for OPTICHAMBER ADVANTAGE ANTI-STATIC VALVED HOLDING CHAMBER is CAF.

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 Respironics New Jersey, Inc. 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: CAF)

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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