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FDA 510(k)

NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI.

K-Number: K810939 · 1981-04-23

ApplicantAllied Healthcare Products, Inc.
Decision Date1981-04-23
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI. is the device name listed in this FDA 510(k) record. The listed applicant is Allied Healthcare Products, Inc.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810939. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI.?

NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI. is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Allied Healthcare Products, Inc.. The 510(k) number is K810939.

When did NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI. receive FDA 510(k) clearance?

NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI. received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810939.

Who is the listed applicant for NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI.?

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

What is the FDA product code for NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI.?

The FDA product code for NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI. is BTT.

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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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