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FDA 510(k)

HEWLETT-PACKARD MODEL M1016A CO2 & M1017A FI02

K-Number: K896030 · 1989-12-22

ApplicantHewlett-Packard Co.
Decision Date1989-12-22
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HEWLETT-PACKARD MODEL M1016A CO2 & M1017A FI02 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 1989-12-22 under 510(k) number K896030. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEWLETT-PACKARD MODEL M1016A CO2 & M1017A FI02?

HEWLETT-PACKARD MODEL M1016A CO2 & M1017A FI02 is a medical device that received FDA 510(k) clearance on 1989-12-22. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K896030.

When did HEWLETT-PACKARD MODEL M1016A CO2 & M1017A FI02 receive FDA 510(k) clearance?

HEWLETT-PACKARD MODEL M1016A CO2 & M1017A FI02 received FDA 510(k) clearance on 1989-12-22, under 510(k) number K896030.

Who is the listed applicant for HEWLETT-PACKARD MODEL M1016A CO2 & M1017A FI02?

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 HEWLETT-PACKARD MODEL M1016A CO2 & M1017A FI02?

The FDA product code for HEWLETT-PACKARD MODEL M1016A CO2 & M1017A FI02 is CCK.

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Related Devices (Code: CCK)

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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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