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FDA 510(k)

HEWLETT-PACKARD MODELS M1400A, M1402A & M1401A

K-Number: K911139 · 1991-06-11

ApplicantHewlett-Packard Co.
Decision Date1991-06-11
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEWLETT-PACKARD MODELS M1400A, M1402A & M1401A 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 1991-06-11 under 510(k) number K911139. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEWLETT-PACKARD MODELS M1400A, M1402A & M1401A?

HEWLETT-PACKARD MODELS M1400A, M1402A & M1401A is a medical device that received FDA 510(k) clearance on 1991-06-11. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K911139.

When did HEWLETT-PACKARD MODELS M1400A, M1402A & M1401A receive FDA 510(k) clearance?

HEWLETT-PACKARD MODELS M1400A, M1402A & M1401A received FDA 510(k) clearance on 1991-06-11, under 510(k) number K911139.

Who is the listed applicant for HEWLETT-PACKARD MODELS M1400A, M1402A & M1401A?

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 MODELS M1400A, M1402A & M1401A?

The FDA product code for HEWLETT-PACKARD MODELS M1400A, M1402A & M1401A is DRT.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: DRT)

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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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