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FDA 510(k)

NEBULIZER SET-2C7105

K-Number: K772222 · 1977-12-22

ApplicantTravenol Laboratories, S.A.
Decision Date1977-12-22
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER SET-2C7105 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 1977-12-22 under 510(k) number K772222. 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 NEBULIZER SET-2C7105?

NEBULIZER SET-2C7105 is a medical device that received FDA 510(k) clearance on 1977-12-22. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K772222.

When did NEBULIZER SET-2C7105 receive FDA 510(k) clearance?

NEBULIZER SET-2C7105 received FDA 510(k) clearance on 1977-12-22, under 510(k) number K772222.

Who is the listed applicant for NEBULIZER SET-2C7105?

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 NEBULIZER SET-2C7105?

The FDA product code for NEBULIZER SET-2C7105 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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