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FDA 510(k)

HP 77010CF

K-Number: K943634 · 1994-09-30

ApplicantHewlett-Packard Co.
Decision Date1994-09-30
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HP 77010CF 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 1994-09-30 under 510(k) number K943634. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP 77010CF?

HP 77010CF is a medical device that received FDA 510(k) clearance on 1994-09-30. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K943634.

When did HP 77010CF receive FDA 510(k) clearance?

HP 77010CF received FDA 510(k) clearance on 1994-09-30, under 510(k) number K943634.

Who is the listed applicant for HP 77010CF?

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 HP 77010CF?

The FDA product code for HP 77010CF is IYO.

Other records listing Hewlett-Packard 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.

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