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FDA 510(k)

DISPOSABLE HUMIDIFIER

K-Number: K760938 · 1976-11-09

ApplicantTravenol Laboratories, S.A.
Decision Date1976-11-09
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE HUMIDIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1976-11-09 under 510(k) number K760938. 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 DISPOSABLE HUMIDIFIER?

DISPOSABLE HUMIDIFIER is a medical device that received FDA 510(k) clearance on 1976-11-09. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K760938.

When did DISPOSABLE HUMIDIFIER receive FDA 510(k) clearance?

DISPOSABLE HUMIDIFIER received FDA 510(k) clearance on 1976-11-09, under 510(k) number K760938.

Who is the listed applicant for DISPOSABLE HUMIDIFIER?

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

What is the FDA product code for DISPOSABLE HUMIDIFIER?

The FDA product code for DISPOSABLE HUMIDIFIER is BTT.

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Other records listing Travenol Laboratories, S.A. as applicant

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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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