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FDA 510(k)

NEBULIZATION KIT & ADAPTER KIT

K-Number: K780264 · 1978-03-09

ApplicantChesebrough-Pond'S U.S.A. Co.
Decision Date1978-03-09
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZATION KIT & ADAPTER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1978-03-09 under 510(k) number K780264. 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 NEBULIZATION KIT & ADAPTER KIT?

NEBULIZATION KIT & ADAPTER KIT is a medical device that received FDA 510(k) clearance on 1978-03-09. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K780264.

When did NEBULIZATION KIT & ADAPTER KIT receive FDA 510(k) clearance?

NEBULIZATION KIT & ADAPTER KIT received FDA 510(k) clearance on 1978-03-09, under 510(k) number K780264.

Who is the listed applicant for NEBULIZATION KIT & ADAPTER KIT?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEBULIZATION KIT & ADAPTER KIT?

The FDA product code for NEBULIZATION KIT & ADAPTER KIT 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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