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FDA 510(k)

IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA-

K-Number: K792373 · 1980-02-13

ApplicantIpco Corp.
Decision Date1980-02-13
Product CodeDXK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA- is the device name listed in this FDA 510(k) record. The listed applicant is Ipco Corp.. It received FDA 510(k) clearance on 1980-02-13 under 510(k) number K792373. The device is classified under product code DXK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA-?

IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA- is a medical device that received FDA 510(k) clearance on 1980-02-13. The listed applicant is Ipco Corp.. The 510(k) number is K792373.

When did IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA- receive FDA 510(k) clearance?

IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA- received FDA 510(k) clearance on 1980-02-13, under 510(k) number K792373.

Who is the listed applicant for IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA-?

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

What is the FDA product code for IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA-?

The FDA product code for IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA- is DXK.

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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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