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FDA 510(k)

RESPIRATORY THERAPY SOLUTIONS - FLEXIBLE

K-Number: K780385 · 1978-05-16

ApplicantTravenol Laboratories, S.A.
Decision Date1978-05-16
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRATORY THERAPY SOLUTIONS - FLEXIBLE 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 1978-05-16 under 510(k) number K780385. 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 RESPIRATORY THERAPY SOLUTIONS - FLEXIBLE?

RESPIRATORY THERAPY SOLUTIONS - FLEXIBLE is a medical device that received FDA 510(k) clearance on 1978-05-16. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K780385.

When did RESPIRATORY THERAPY SOLUTIONS - FLEXIBLE receive FDA 510(k) clearance?

RESPIRATORY THERAPY SOLUTIONS - FLEXIBLE received FDA 510(k) clearance on 1978-05-16, under 510(k) number K780385.

Who is the listed applicant for RESPIRATORY THERAPY SOLUTIONS - FLEXIBLE?

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 RESPIRATORY THERAPY SOLUTIONS - FLEXIBLE?

The FDA product code for RESPIRATORY THERAPY SOLUTIONS - FLEXIBLE 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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