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FDA 510(k)

MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT

K-Number: K843934 · 1984-11-20

ApplicantFuture Impex Corp.
Decision Date1984-11-20
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Future Impex Corp.. It received FDA 510(k) clearance on 1984-11-20 under 510(k) number K843934. 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 MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT?

MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT is a medical device that received FDA 510(k) clearance on 1984-11-20. The listed applicant is Future Impex Corp.. The 510(k) number is K843934.

When did MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT receive FDA 510(k) clearance?

MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT received FDA 510(k) clearance on 1984-11-20, under 510(k) number K843934.

Who is the listed applicant for MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT?

The FDA 510(k) record lists Future Impex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT?

The FDA product code for MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT is DPS.

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Other records listing Future Impex Corp. 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.

K861487ST-90 SPIRO ANALIZERK854686TE-25 COAGURO METERK854687ERMA HB-METER MODEL 303NK854685DIGITAL-9 KEY LEUCOCYTE COUNTERK854677ERMA PC-604 BLOOD CELL COUNTERK854678ERMA PC-602 PC-603 BLOOD CELL COUNTER

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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.

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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