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FDA 510(k)

HOLTER PERFORMER FEATHER WEIGHT/CASS

K-Number: K833823 · 1983-12-01

ApplicantApplied Cardiac Systems
Decision Date1983-12-01
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HOLTER PERFORMER FEATHER WEIGHT/CASS is the device name listed in this FDA 510(k) record. The listed applicant is Applied Cardiac Systems. It received FDA 510(k) clearance on 1983-12-01 under 510(k) number K833823. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOLTER PERFORMER FEATHER WEIGHT/CASS?

HOLTER PERFORMER FEATHER WEIGHT/CASS is a medical device that received FDA 510(k) clearance on 1983-12-01. The listed applicant is Applied Cardiac Systems. The 510(k) number is K833823.

When did HOLTER PERFORMER FEATHER WEIGHT/CASS receive FDA 510(k) clearance?

HOLTER PERFORMER FEATHER WEIGHT/CASS received FDA 510(k) clearance on 1983-12-01, under 510(k) number K833823.

Who is the listed applicant for HOLTER PERFORMER FEATHER WEIGHT/CASS?

The FDA 510(k) record lists Applied Cardiac Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOLTER PERFORMER FEATHER WEIGHT/CASS?

The FDA product code for HOLTER PERFORMER FEATHER WEIGHT/CASS is DSH.

Related Clinical Trials

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.

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Other records listing Applied Cardiac Systems 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.

K042413ACS MODEL NCP-2K860249THE HOLTER REPORTER (TM)K813602HOLTER PERFORMER

Related Devices (Code: DSH)

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.

K260157LifeLens Physiological MonitorLifeLens Technologies, Inc.K252389Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)Smwmed, Inc.K253293VitaloJAK Clinic (Model 7100)Vitalograph , Ltd.K243650Zio® monitor (DFG0001)iRhythm Technologies, Inc.K243603AeviceMDAevice Health Pte. , Ltd.K242583AT-Patch (ATP-C130/ATP-C70)Atsens Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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