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FDA 510(k)

APNEA/BRADYCARDIA MONITOR HB 95

K-Number: K830666 · 1983-07-18

ApplicantHarvey-Bostwick, Inc.
Decision Date1983-07-18
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

APNEA/BRADYCARDIA MONITOR HB 95 is the device name listed in this FDA 510(k) record. The listed applicant is Harvey-Bostwick, Inc.. It received FDA 510(k) clearance on 1983-07-18 under 510(k) number K830666. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APNEA/BRADYCARDIA MONITOR HB 95?

APNEA/BRADYCARDIA MONITOR HB 95 is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is Harvey-Bostwick, Inc.. The 510(k) number is K830666.

When did APNEA/BRADYCARDIA MONITOR HB 95 receive FDA 510(k) clearance?

APNEA/BRADYCARDIA MONITOR HB 95 received FDA 510(k) clearance on 1983-07-18, under 510(k) number K830666.

Who is the listed applicant for APNEA/BRADYCARDIA MONITOR HB 95?

The FDA 510(k) record lists Harvey-Bostwick, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APNEA/BRADYCARDIA MONITOR HB 95?

The FDA product code for APNEA/BRADYCARDIA MONITOR HB 95 is DPS.

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 Harvey-Bostwick, Inc. 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.

K821942HARVEY-BOSTWICK BRADY CARDIA MONIT. HB85

Related Devices (Code: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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