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FDA 510(k)

DETECTOR, MODEL 79875A, VARIABLE

K-Number: K781771 · 1978-12-20

ApplicantHewlett-Packard Co.
Decision Date1978-12-20
Product CodeKIE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DETECTOR, MODEL 79875A, VARIABLE 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 1978-12-20 under 510(k) number K781771. The device is classified under product code KIE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DETECTOR, MODEL 79875A, VARIABLE?

DETECTOR, MODEL 79875A, VARIABLE is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K781771.

When did DETECTOR, MODEL 79875A, VARIABLE receive FDA 510(k) clearance?

DETECTOR, MODEL 79875A, VARIABLE received FDA 510(k) clearance on 1978-12-20, under 510(k) number K781771.

Who is the listed applicant for DETECTOR, MODEL 79875A, VARIABLE?

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 DETECTOR, MODEL 79875A, VARIABLE?

The FDA product code for DETECTOR, MODEL 79875A, VARIABLE is KIE.

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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: KIE)

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.

K964588WATERS 515 HPLC PUMP (515)Waters CorporationK935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPThe Perkin-Elmer Corp.K924347WATERS(TM) 996 PDAMillipore Corp.K914841CHROMATOGRAPHY CLINICAL USE 75JQRMillipore Corp.K911299EQUIPMENT/MATERIAL DECONTAMINATING KITRohm and Haas Co.K862506THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORMillipore 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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