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FDA 510(k)

NEBULIZER TUBING SET

K-Number: K800083 · 1980-01-24

ApplicantAbbott Laboratories
Decision Date1980-01-24
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1980-01-24 under 510(k) number K800083. 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 TUBING SET?

NEBULIZER TUBING SET is a medical device that received FDA 510(k) clearance on 1980-01-24. The listed applicant is Abbott Laboratories. The 510(k) number is K800083.

When did NEBULIZER TUBING SET receive FDA 510(k) clearance?

NEBULIZER TUBING SET received FDA 510(k) clearance on 1980-01-24, under 510(k) number K800083.

Who is the listed applicant for NEBULIZER TUBING SET?

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

What is the FDA product code for NEBULIZER TUBING SET?

The FDA product code for NEBULIZER TUBING SET 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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