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FDA 510(k)

3390A REPORTING INTEGRATOR

K-Number: K802031 · 1980-09-16

ApplicantHewlett-Packard Co.
Decision Date1980-09-16
Product CodeLDM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

3390A REPORTING INTEGRATOR 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 1980-09-16 under 510(k) number K802031. The device is classified under product code LDM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3390A REPORTING INTEGRATOR?

3390A REPORTING INTEGRATOR is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K802031.

When did 3390A REPORTING INTEGRATOR receive FDA 510(k) clearance?

3390A REPORTING INTEGRATOR received FDA 510(k) clearance on 1980-09-16, under 510(k) number K802031.

Who is the listed applicant for 3390A REPORTING INTEGRATOR?

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 3390A REPORTING INTEGRATOR?

The FDA product code for 3390A REPORTING INTEGRATOR is LDM.

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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: LDM)

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.

K960392CDMBio-RadK961557ALLIANCE 2690 SEPARATIONS MODULEWaters CorporationK942451BIO-RAD CLINICAL DATA MANAGEMENT SYSTEMBio-RadK922388WATERS(TM) LC MODULE I FOR CLINICAL USEMillipore Corp.K920136WATERS 717 AUTOSAMPLERMillipore Corp.K903647MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETEMillipore Corp.

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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