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FDA 510(k)

MICROMED QRS CARD

K-Number: K903722 · 1990-12-05

ApplicantNasiff Assoc., Inc.
Decision Date1990-12-05
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROMED QRS CARD is the device name listed in this FDA 510(k) record. The listed applicant is Nasiff Assoc., Inc.. It received FDA 510(k) clearance on 1990-12-05 under 510(k) number K903722. 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 MICROMED QRS CARD?

MICROMED QRS CARD is a medical device that received FDA 510(k) clearance on 1990-12-05. The listed applicant is Nasiff Assoc., Inc.. The 510(k) number is K903722.

When did MICROMED QRS CARD receive FDA 510(k) clearance?

MICROMED QRS CARD received FDA 510(k) clearance on 1990-12-05, under 510(k) number K903722.

Who is the listed applicant for MICROMED QRS CARD?

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

What is the FDA product code for MICROMED QRS CARD?

The FDA product code for MICROMED QRS CARD is DPS.

Related Clinical Trials

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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Other records listing Nasiff Assoc., 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.

K993616CARDIO-CARD INTERPRETATION SYSTEM IK972795CARDIO-CARD MANAGEMENT SYSTEM IIK960544CARDIO-CARD HOLTER ECG MANAGEMENT SYSTEMK920020CARDIO-CARD ECG MANAGEMENT SYSTEM

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

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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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