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FDA 510(k)

3388 REPORTING INTEGRATOR

K-Number: K792158 · 1979-11-16

ApplicantHewlett-Packard Co.
Decision Date1979-11-16
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

3388 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 1979-11-16 under 510(k) number K792158. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3388 REPORTING INTEGRATOR?

3388 REPORTING INTEGRATOR is a medical device that received FDA 510(k) clearance on 1979-11-16. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K792158.

When did 3388 REPORTING INTEGRATOR receive FDA 510(k) clearance?

3388 REPORTING INTEGRATOR received FDA 510(k) clearance on 1979-11-16, under 510(k) number K792158.

Who is the listed applicant for 3388 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 3388 REPORTING INTEGRATOR?

The FDA product code for 3388 REPORTING INTEGRATOR is JQP.

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Other records listing Hewlett-Packard Co. as applicant

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.

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: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, 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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