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FDA 510(k)

SOLUTIONS FOR RESPIRATORY THERAPY

K-Number: K780668 · 1978-06-13

ApplicantTravenol Laboratories, S.A.
Decision Date1978-06-13
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SOLUTIONS FOR RESPIRATORY THERAPY 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 1978-06-13 under 510(k) number K780668. 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 SOLUTIONS FOR RESPIRATORY THERAPY?

SOLUTIONS FOR RESPIRATORY THERAPY is a medical device that received FDA 510(k) clearance on 1978-06-13. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K780668.

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

SOLUTIONS FOR RESPIRATORY THERAPY received FDA 510(k) clearance on 1978-06-13, under 510(k) number K780668.

Who is the listed applicant for SOLUTIONS FOR RESPIRATORY THERAPY?

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 SOLUTIONS FOR RESPIRATORY THERAPY?

The FDA product code for SOLUTIONS FOR RESPIRATORY THERAPY 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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