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FDA 510(k)

EKG ACQUISITION & ANALYSIS CART

K-Number: K772353 · 1978-01-06

ApplicantIntl. Business Machines
Decision Date1978-01-06
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

EKG ACQUISITION & ANALYSIS CART is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Business Machines. It received FDA 510(k) clearance on 1978-01-06 under 510(k) number K772353. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EKG ACQUISITION & ANALYSIS CART?

EKG ACQUISITION & ANALYSIS CART is a medical device that received FDA 510(k) clearance on 1978-01-06. The listed applicant is Intl. Business Machines. The 510(k) number is K772353.

When did EKG ACQUISITION & ANALYSIS CART receive FDA 510(k) clearance?

EKG ACQUISITION & ANALYSIS CART received FDA 510(k) clearance on 1978-01-06, under 510(k) number K772353.

Who is the listed applicant for EKG ACQUISITION & ANALYSIS CART?

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

What is the FDA product code for EKG ACQUISITION & ANALYSIS CART?

The FDA product code for EKG ACQUISITION & ANALYSIS CART is LOS.

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Other records listing Intl. Business Machines 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.

K831004AUTOMATED 8400 BLOOD CELL SEPARATORK830163IBM 588 DIGITAL ECG ACQUISITION/ANALYSISK812355IBM 2991 BLOOD CELL PROCESSOR MOD. 1 & 2K810989IBM 5880 ACQUISITION & ANALYSIS CART TELK810988IBM 5885 DIGITAL ECG ACQUISITION CARTK771258BLOOD CELL SEPARATOR 2997

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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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