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FDA 510(k)

NEBULIZER ADAPTER (AERMIST)

K-Number: K760442 · 1976-08-26

ApplicantAerway Laboratories, Inc.
Decision Date1976-08-26
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER ADAPTER (AERMIST) is the device name listed in this FDA 510(k) record. The listed applicant is Aerway Laboratories, Inc.. It received FDA 510(k) clearance on 1976-08-26 under 510(k) number K760442. 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 NEBULIZER ADAPTER (AERMIST)?

NEBULIZER ADAPTER (AERMIST) is a medical device that received FDA 510(k) clearance on 1976-08-26. The listed applicant is Aerway Laboratories, Inc.. The 510(k) number is K760442.

When did NEBULIZER ADAPTER (AERMIST) receive FDA 510(k) clearance?

NEBULIZER ADAPTER (AERMIST) received FDA 510(k) clearance on 1976-08-26, under 510(k) number K760442.

Who is the listed applicant for NEBULIZER ADAPTER (AERMIST)?

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

What is the FDA product code for NEBULIZER ADAPTER (AERMIST)?

The FDA product code for NEBULIZER ADAPTER (AERMIST) is CAF.

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Official Source

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