HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE

FDA 510(k) Premarket Notification · Submission K903523 · Applicant: Hewlett-Packard Co.

Public Record 510(k) Submission Decision Date: 1990-10-23 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K903523.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K903523
Applicant / Sponsor
Device Name
HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE
Product Code
DQA
Decision Date
1990-10-23
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Cardiovascular (CV)
Clearance Type
Traditional
Third Party Flag
N
Date Received
1990-08-06

Related Establishments / Registrations

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