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FDA 510(k)

5300 PERCUSSOR

K-Number: K790675 · 1979-04-18

ApplicantHudson Oxygen Therapy Sales Co.
Decision Date1979-04-18
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

5300 PERCUSSOR is the device name listed in this FDA 510(k) record. The listed applicant is Hudson Oxygen Therapy Sales Co.. It received FDA 510(k) clearance on 1979-04-18 under 510(k) number K790675. The device is classified under product code BYI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 5300 PERCUSSOR?

5300 PERCUSSOR is a medical device that received FDA 510(k) clearance on 1979-04-18. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K790675.

When did 5300 PERCUSSOR receive FDA 510(k) clearance?

5300 PERCUSSOR received FDA 510(k) clearance on 1979-04-18, under 510(k) number K790675.

Who is the listed applicant for 5300 PERCUSSOR?

The FDA 510(k) record lists Hudson Oxygen Therapy Sales Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 5300 PERCUSSOR?

The FDA product code for 5300 PERCUSSOR is BYI.

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Other records listing Hudson Oxygen Therapy Sales Co. as applicant

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Related Devices (Code: BYI)

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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