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FDA 510(k)

DISPOS. MEDICATION NEBULIZER

K-Number: K831270 · 1983-06-08

ApplicantHospitak, Inc.
Decision Date1983-06-08
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOS. MEDICATION NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Hospitak, Inc.. It received FDA 510(k) clearance on 1983-06-08 under 510(k) number K831270. 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 DISPOS. MEDICATION NEBULIZER?

DISPOS. MEDICATION NEBULIZER is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Hospitak, Inc.. The 510(k) number is K831270.

When did DISPOS. MEDICATION NEBULIZER receive FDA 510(k) clearance?

DISPOS. MEDICATION NEBULIZER received FDA 510(k) clearance on 1983-06-08, under 510(k) number K831270.

Who is the listed applicant for DISPOS. MEDICATION NEBULIZER?

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

What is the FDA product code for DISPOS. MEDICATION NEBULIZER?

The FDA product code for DISPOS. MEDICATION 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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