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FDA 510(k)

DISPOS. PRESSURE KIT 1295K SERIES

K-Number: K843273 · 1985-06-11

ApplicantHewlett-Packard Co.
Decision Date1985-06-11
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOS. PRESSURE KIT 1295K SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1985-06-11 under 510(k) number K843273. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOS. PRESSURE KIT 1295K SERIES?

DISPOS. PRESSURE KIT 1295K SERIES is a medical device that received FDA 510(k) clearance on 1985-06-11. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K843273.

When did DISPOS. PRESSURE KIT 1295K SERIES receive FDA 510(k) clearance?

DISPOS. PRESSURE KIT 1295K SERIES received FDA 510(k) clearance on 1985-06-11, under 510(k) number K843273.

Who is the listed applicant for DISPOS. PRESSURE KIT 1295K SERIES?

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

What is the FDA product code for DISPOS. PRESSURE KIT 1295K SERIES?

The FDA product code for DISPOS. PRESSURE KIT 1295K SERIES is DRS.

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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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