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FDA 510(k)

ACCUSTRESS EXERCISE TESTING SYSTEM

K-Number: K953127 · 1996-02-29

ApplicantHewlett-Packard Co.
Decision Date1996-02-29
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACCUSTRESS EXERCISE TESTING SYSTEM 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 1996-02-29 under 510(k) number K953127. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUSTRESS EXERCISE TESTING SYSTEM?

ACCUSTRESS EXERCISE TESTING SYSTEM is a medical device that received FDA 510(k) clearance on 1996-02-29. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K953127.

When did ACCUSTRESS EXERCISE TESTING SYSTEM receive FDA 510(k) clearance?

ACCUSTRESS EXERCISE TESTING SYSTEM received FDA 510(k) clearance on 1996-02-29, under 510(k) number K953127.

Who is the listed applicant for ACCUSTRESS EXERCISE TESTING SYSTEM?

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 ACCUSTRESS EXERCISE TESTING SYSTEM?

The FDA product code for ACCUSTRESS EXERCISE TESTING SYSTEM is DQK.

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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: DQK)

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.

K261729EnSite™ X EP SystemAbbott MedicalK262005Affera Integrated Mapping SystemMedtronic, Inc.K253692AVVIGO™+ Multi-Modality Guidance SystemBoston ScientificK253576CorVista System® with PCWP Add-OnAnalytics For Life, Inc.K262006EnSite™ X EP SystemAbbott MedicalK252978ScioCardio ECG Analysis PlatformSynergen Technology Labs, LLC

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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