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FDA 510(k)

MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG

K-Number: K913827 · 1991-11-19

ApplicantHewlett-Packard Co.
Decision Date1991-11-19
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG 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 1991-11-19 under 510(k) number K913827. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG?

MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG is a medical device that received FDA 510(k) clearance on 1991-11-19. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K913827.

When did MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG receive FDA 510(k) clearance?

MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG received FDA 510(k) clearance on 1991-11-19, under 510(k) number K913827.

Who is the listed applicant for MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG?

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 MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG?

The FDA product code for MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG is DPW.

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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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