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FDA 510(k)

U-MID PREFILLED NEBULIZER

K-Number: K760585 · 1976-10-15

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1976-10-15
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

U-MID PREFILLED NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1976-10-15 under 510(k) number K760585. 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 U-MID PREFILLED NEBULIZER?

U-MID PREFILLED NEBULIZER is a medical device that received FDA 510(k) clearance on 1976-10-15. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K760585.

When did U-MID PREFILLED NEBULIZER receive FDA 510(k) clearance?

U-MID PREFILLED NEBULIZER received FDA 510(k) clearance on 1976-10-15, under 510(k) number K760585.

Who is the listed applicant for U-MID PREFILLED NEBULIZER?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for U-MID PREFILLED NEBULIZER?

The FDA product code for U-MID PREFILLED NEBULIZER is CAF.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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