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FDA 510(k)

C150-P ECG CABLES

K-Number: K870926 · 1987-05-21

ApplicantDesco Industries, Inc.
Decision Date1987-05-21
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

C150-P ECG CABLES is the device name listed in this FDA 510(k) record. The listed applicant is Desco Industries, Inc.. It received FDA 510(k) clearance on 1987-05-21 under 510(k) number K870926. 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 C150-P ECG CABLES?

C150-P ECG CABLES is a medical device that received FDA 510(k) clearance on 1987-05-21. The listed applicant is Desco Industries, Inc.. The 510(k) number is K870926.

When did C150-P ECG CABLES receive FDA 510(k) clearance?

C150-P ECG CABLES received FDA 510(k) clearance on 1987-05-21, under 510(k) number K870926.

Who is the listed applicant for C150-P ECG CABLES?

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

What is the FDA product code for C150-P ECG CABLES?

The FDA product code for C150-P ECG CABLES is DPS.

Related Clinical Trials

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Other records listing Desco Industries, 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.

K873492BSK-1033 TELEMETRY MONITORING CABLEK873608TENS LEAD

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

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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