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FDA 510(k)

HEWLETT-PACKARD MODELS 78354A & 78352A PULSE OXI.

K-Number: K881136 · 1988-05-18

ApplicantHewlett-Packard Co.
Decision Date1988-05-18
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEWLETT-PACKARD MODELS 78354A & 78352A PULSE OXI. 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 1988-05-18 under 510(k) number K881136. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEWLETT-PACKARD MODELS 78354A & 78352A PULSE OXI.?

HEWLETT-PACKARD MODELS 78354A & 78352A PULSE OXI. is a medical device that received FDA 510(k) clearance on 1988-05-18. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K881136.

When did HEWLETT-PACKARD MODELS 78354A & 78352A PULSE OXI. receive FDA 510(k) clearance?

HEWLETT-PACKARD MODELS 78354A & 78352A PULSE OXI. received FDA 510(k) clearance on 1988-05-18, under 510(k) number K881136.

Who is the listed applicant for HEWLETT-PACKARD MODELS 78354A & 78352A PULSE OXI.?

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 78354A & 78352A PULSE OXI.?

The FDA product code for HEWLETT-PACKARD MODELS 78354A & 78352A PULSE OXI. is DQA.

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Related Devices (Code: DQA)

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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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