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FDA 510(k)

HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA

K-Number: K844484 · 1985-07-24

ApplicantVitatron Medical BV
Decision Date1985-07-24
Product CodeKRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA is the device name listed in this FDA 510(k) record. The listed applicant is Vitatron Medical BV. It received FDA 510(k) clearance on 1985-07-24 under 510(k) number K844484. The device is classified under product code KRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA?

HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA is a medical device that received FDA 510(k) clearance on 1985-07-24. The listed applicant is Vitatron Medical BV. The 510(k) number is K844484.

When did HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA receive FDA 510(k) clearance?

HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA received FDA 510(k) clearance on 1985-07-24, under 510(k) number K844484.

Who is the listed applicant for HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA?

The FDA 510(k) record lists Vitatron Medical BV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA?

The FDA product code for HEWLETT PACKARDT HP 85 W/ VITATRON PH1 PROGRAM HEA is KRG.

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Other records listing Vitatron Medical BV 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.

K854790CERYX PACEMAKER MODELS 114, 314 & 614K844485CERYX6, 611, CERYX 3 311 & CERYX 1 111K844483TP 1K840668ELECTRODE PACEMAKER, PERM & TEMPK831859PACEMAKER PROGRAMMER #2032K831860GENERATOR, PULSE, PACEMAKER #532

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Related Devices (Code: KRG)

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.

K933278INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04Intermedics, Inc.K884522MODEL 5650 OPTIMATE PERSONAL PROGRAMMERTeletronics, Inc.K880738MODEL 2331T PATIENT PROGRAMMERMedtronic VascularK882429MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004Tpl-Cordis, Inc.K864712MODEL 1740 PERSONAL POCKET PROGRAMMERTelectronics, Inc.K871986MODEL 5600B PROGRAMMER, PACEMAKERTelectronics, 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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