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FDA 510(k)

LOGIC 3 ELECTROCARDIOGRAPH

K-Number: K882472 · 1988-11-17

ApplicantCel-Med Co., Inc.
Decision Date1988-11-17
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LOGIC 3 ELECTROCARDIOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Cel-Med Co., Inc.. It received FDA 510(k) clearance on 1988-11-17 under 510(k) number K882472. 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 LOGIC 3 ELECTROCARDIOGRAPH?

LOGIC 3 ELECTROCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 1988-11-17. The listed applicant is Cel-Med Co., Inc.. The 510(k) number is K882472.

When did LOGIC 3 ELECTROCARDIOGRAPH receive FDA 510(k) clearance?

LOGIC 3 ELECTROCARDIOGRAPH received FDA 510(k) clearance on 1988-11-17, under 510(k) number K882472.

Who is the listed applicant for LOGIC 3 ELECTROCARDIOGRAPH?

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

What is the FDA product code for LOGIC 3 ELECTROCARDIOGRAPH?

The FDA product code for LOGIC 3 ELECTROCARDIOGRAPH is DPS.

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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.

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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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