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FDA 510(k)

SHERWOOD NEBULIZER KIT

K-Number: K791089 · 1979-07-10

ApplicantSherwood Medical Co.
Decision Date1979-07-10
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SHERWOOD NEBULIZER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1979-07-10 under 510(k) number K791089. 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 SHERWOOD NEBULIZER KIT?

SHERWOOD NEBULIZER KIT is a medical device that received FDA 510(k) clearance on 1979-07-10. The listed applicant is Sherwood Medical Co.. The 510(k) number is K791089.

When did SHERWOOD NEBULIZER KIT receive FDA 510(k) clearance?

SHERWOOD NEBULIZER KIT received FDA 510(k) clearance on 1979-07-10, under 510(k) number K791089.

Who is the listed applicant for SHERWOOD NEBULIZER KIT?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHERWOOD NEBULIZER KIT?

The FDA product code for SHERWOOD NEBULIZER KIT is CAF.

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Other records listing Sherwood Medical Co. as applicant

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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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