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FDA 510(k)

SINGLE & DUAL CHANNEL RECORDER

K-Number: K772048 · 1977-11-09

ApplicantHewlett-Packard Co.
Decision Date1977-11-09
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SINGLE & DUAL CHANNEL RECORDER 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 1977-11-09 under 510(k) number K772048. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE & DUAL CHANNEL RECORDER?

SINGLE & DUAL CHANNEL RECORDER is a medical device that received FDA 510(k) clearance on 1977-11-09. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K772048.

When did SINGLE & DUAL CHANNEL RECORDER receive FDA 510(k) clearance?

SINGLE & DUAL CHANNEL RECORDER received FDA 510(k) clearance on 1977-11-09, under 510(k) number K772048.

Who is the listed applicant for SINGLE & DUAL CHANNEL RECORDER?

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 SINGLE & DUAL CHANNEL RECORDER?

The FDA product code for SINGLE & DUAL CHANNEL RECORDER is DSF.

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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: DSF)

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.

K910871EDENTEC DIGITAL CHARTER MODEL 3710Edentec Corp.K912929DASH IVAstro-Med, Inc.K905856MODEL 556 MONITORGe Medical Systems Information TechnologiesK902586GRI LASERGRAPH(TM) ECG PAPERGri Medical Products, Inc.K902230COLORADO COLOR IMAGING RECORDERHoneywell, Inc.K901385GABRIEL MEDICAL CLS THERMAL RECORDERGabriel Medical, 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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