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FDA 510(k)

2C 7140 HEATED HUMIDIFER CANNISTER

K-Number: K802145 · 1980-09-26

ApplicantTravenol Laboratories, S.A.
Decision Date1980-09-26
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

2C 7140 HEATED HUMIDIFER CANNISTER 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 1980-09-26 under 510(k) number K802145. 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 2C 7140 HEATED HUMIDIFER CANNISTER?

2C 7140 HEATED HUMIDIFER CANNISTER is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K802145.

When did 2C 7140 HEATED HUMIDIFER CANNISTER receive FDA 510(k) clearance?

2C 7140 HEATED HUMIDIFER CANNISTER received FDA 510(k) clearance on 1980-09-26, under 510(k) number K802145.

Who is the listed applicant for 2C 7140 HEATED HUMIDIFER CANNISTER?

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 2C 7140 HEATED HUMIDIFER CANNISTER?

The FDA product code for 2C 7140 HEATED HUMIDIFER CANNISTER is BTT.

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

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Related Devices (Code: BTT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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