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FDA 510(k)

N-CHANNEL

K-Number: K834212 · 1984-11-13

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1984-11-13
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

N-CHANNEL is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1984-11-13 under 510(k) number K834212. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N-CHANNEL?

N-CHANNEL is a medical device that received FDA 510(k) clearance on 1984-11-13. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K834212.

When did N-CHANNEL receive FDA 510(k) clearance?

N-CHANNEL received FDA 510(k) clearance on 1984-11-13, under 510(k) number K834212.

Who is the listed applicant for N-CHANNEL?

The FDA 510(k) record lists Philips Medical Systems (Cleveland), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for N-CHANNEL?

The FDA product code for N-CHANNEL is LOS.

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Other records listing Philips Medical Systems (Cleveland), Inc. as applicant

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Related Devices (Code: LOS)

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.

K090895EKG-PLUS II SOFTWAREBionet Co., Ltd.K083749CARDIOVIEW32 REVIEW MODULEQrs Diagnostic, LLCK073376PHILIPS ECG ALGORITHMPhilips Medical SystemsK023034CARDIOTOUCH-3000Bionet Company, Ltd.K011328CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPHBionet Company, Ltd.K993616CARDIO-CARD INTERPRETATION SYSTEM INasiff Assoc., 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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