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FDA 510(k)

SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM

K-Number: K922221 · 1993-04-21

ApplicantDel Mar Avionics
Decision Date1993-04-21
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Del Mar Avionics. It received FDA 510(k) clearance on 1993-04-21 under 510(k) number K922221. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM?

SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM is a medical device that received FDA 510(k) clearance on 1993-04-21. The listed applicant is Del Mar Avionics. The 510(k) number is K922221.

When did SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM receive FDA 510(k) clearance?

SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM received FDA 510(k) clearance on 1993-04-21, under 510(k) number K922221.

Who is the listed applicant for SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM?

The FDA 510(k) record lists Del Mar Avionics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM?

The FDA product code for SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM is LOS.

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Other records listing Del Mar Avionics 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.

K990027OMNICORDER, MODEL 464K971696SENTINEL RECORDER, MODELS 471/472K963174HOLTER DIGICORDER WITH PACER OPTION (MODEL 483)K950020HOLTER PACERCORDER(R)K942653HOLTER SSR DIGICORDER(TM)K896862MODEL 263 SPECTRASCAN(TM) HOLTER ANALYSIS SYSTEM

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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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