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FDA 510(k)

MASTER-NEB NEBULIZER COMPRESSOR SYSTEM

K-Number: K943717 · 1995-09-12

ApplicantHoward K. Mann & Assoc.
Decision Date1995-09-12
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MASTER-NEB NEBULIZER COMPRESSOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howard K. Mann & Assoc.. It received FDA 510(k) clearance on 1995-09-12 under 510(k) number K943717. 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 MASTER-NEB NEBULIZER COMPRESSOR SYSTEM?

MASTER-NEB NEBULIZER COMPRESSOR SYSTEM is a medical device that received FDA 510(k) clearance on 1995-09-12. The listed applicant is Howard K. Mann & Assoc.. The 510(k) number is K943717.

When did MASTER-NEB NEBULIZER COMPRESSOR SYSTEM receive FDA 510(k) clearance?

MASTER-NEB NEBULIZER COMPRESSOR SYSTEM received FDA 510(k) clearance on 1995-09-12, under 510(k) number K943717.

Who is the listed applicant for MASTER-NEB NEBULIZER COMPRESSOR SYSTEM?

The FDA 510(k) record lists Howard K. Mann & Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASTER-NEB NEBULIZER COMPRESSOR SYSTEM?

The FDA product code for MASTER-NEB NEBULIZER COMPRESSOR SYSTEM is CAF.

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Official Source

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