FDA 510(k)

HALL ARTERIAL OSCILLATOR

K-Number: K801063 · 1980-09-26

Decision Date1980-09-26

Product CodeDWX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

HALL ARTERIAL OSCILLATOR is the device name listed in this FDA 510(k) record. The listed applicant is American Sterilizer Co.. It received FDA 510(k) clearance on 1980-09-26 under 510(k) number K801063. The device is classified under product code DWX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HALL ARTERIAL OSCILLATOR?

HALL ARTERIAL OSCILLATOR is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is American Sterilizer Co.. The 510(k) number is K801063.

When did HALL ARTERIAL OSCILLATOR receive FDA 510(k) clearance?

HALL ARTERIAL OSCILLATOR received FDA 510(k) clearance on 1980-09-26, under 510(k) number K801063.

Who is the listed applicant for HALL ARTERIAL OSCILLATOR?

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

What is the FDA product code for HALL ARTERIAL OSCILLATOR?

The FDA product code for HALL ARTERIAL OSCILLATOR is DWX.

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Other records listing American Sterilizer Co. as applicant

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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.