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FDA 510(k)

HEWLETT-PACKARD MODEL M1020A PULSE OXIMETER

K-Number: K923343 · 1993-02-10

ApplicantHewlett-Packard Co.
Decision Date1993-02-10
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEWLETT-PACKARD MODEL M1020A PULSE OXIMETER 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 1993-02-10 under 510(k) number K923343. 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 MODEL M1020A PULSE OXIMETER?

HEWLETT-PACKARD MODEL M1020A PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1993-02-10. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K923343.

When did HEWLETT-PACKARD MODEL M1020A PULSE OXIMETER receive FDA 510(k) clearance?

HEWLETT-PACKARD MODEL M1020A PULSE OXIMETER received FDA 510(k) clearance on 1993-02-10, under 510(k) number K923343.

Who is the listed applicant for HEWLETT-PACKARD MODEL M1020A PULSE OXIMETER?

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 MODEL M1020A PULSE OXIMETER?

The FDA product code for HEWLETT-PACKARD MODEL M1020A PULSE OXIMETER is DQA.

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Other records listing Hewlett-Packard Co. as applicant

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K992543HEARTSTREAM XLT DEFIBRILLATOR/MONITOR, AC CHARGER, DC CHARGER, DATA CARD, SINGLE BAY ADAPTER, DEFIBRILLATOR PADS CABLEK993587HP M2376A DEVICE LINK SYSTEMK993169MODIFICATION OF: PHYSIOLOGICAL SIGNAL TRANSMITTER AND RECEIVER, MODEL 3810AK992977HEWLETT PACKARD MULTIFUNCTION PEDIATRIC DEFIB FUNCTION, MODEL M3503A & M3504AK993516HP M2600A VIRIDIA TELEMETRY SYSTEMK993171HP VIRIDIA INFORMATION SYSTEM, MODELS M3150A/ M3151A/ M3153A/ M3154A

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Related Devices (Code: DQA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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