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FDA 510(k)

OPTION A02 MODEL 15202A

K-Number: K830124 · 1983-02-09

ApplicantHewlett-Packard Co.
Decision Date1983-02-09
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OPTION A02 MODEL 15202A 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 1983-02-09 under 510(k) number K830124. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTION A02 MODEL 15202A?

OPTION A02 MODEL 15202A is a medical device that received FDA 510(k) clearance on 1983-02-09. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K830124.

When did OPTION A02 MODEL 15202A receive FDA 510(k) clearance?

OPTION A02 MODEL 15202A received FDA 510(k) clearance on 1983-02-09, under 510(k) number K830124.

Who is the listed applicant for OPTION A02 MODEL 15202A?

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 OPTION A02 MODEL 15202A?

The FDA product code for OPTION A02 MODEL 15202A is CCL.

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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: CCL)

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.

K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter LabsK251245OxyMinder Pro (10310)Bio-Med Device, Inc.K250002Smart Check O2 (MA0236)Life Spark Medical, LLCK221734Maxtec MaxO2 ME+pMaxtec, LLCK213933Percent Oxygen SensorsCareox, LLCK213948OxyMinderBio-Med Devices, Inc.

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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