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FDA 510(k)

HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS

K-Number: K842829 · 1984-10-18

ApplicantNorth American Instrument Corp.
Decision Date1984-10-18
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS is the device name listed in this FDA 510(k) record. The listed applicant is North American Instrument Corp.. It received FDA 510(k) clearance on 1984-10-18 under 510(k) number K842829. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS?

HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS is a medical device that received FDA 510(k) clearance on 1984-10-18. The listed applicant is North American Instrument Corp.. The 510(k) number is K842829.

When did HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS receive FDA 510(k) clearance?

HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS received FDA 510(k) clearance on 1984-10-18, under 510(k) number K842829.

Who is the listed applicant for HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS?

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

What is the FDA product code for HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS?

The FDA product code for HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS is DTL.

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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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