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FDA 510(k)

MICRO MED INC. QRS-CARD(TM) OFFICE ECG MONITOR

K-Number: K914762 · 1991-12-05

ApplicantMicromed
Decision Date1991-12-05
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICRO MED INC. QRS-CARD(TM) OFFICE ECG MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Micromed. It received FDA 510(k) clearance on 1991-12-05 under 510(k) number K914762. 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 MICRO MED INC. QRS-CARD(TM) OFFICE ECG MONITOR?

MICRO MED INC. QRS-CARD(TM) OFFICE ECG MONITOR is a medical device that received FDA 510(k) clearance on 1991-12-05. The listed applicant is Micromed. The 510(k) number is K914762.

When did MICRO MED INC. QRS-CARD(TM) OFFICE ECG MONITOR receive FDA 510(k) clearance?

MICRO MED INC. QRS-CARD(TM) OFFICE ECG MONITOR received FDA 510(k) clearance on 1991-12-05, under 510(k) number K914762.

Who is the listed applicant for MICRO MED INC. QRS-CARD(TM) OFFICE ECG MONITOR?

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

What is the FDA product code for MICRO MED INC. QRS-CARD(TM) OFFICE ECG MONITOR?

The FDA product code for MICRO MED INC. QRS-CARD(TM) OFFICE ECG MONITOR 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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