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FDA 510(k)

SCANNER, ULTRASOUND BODY/HEART

K-Number: K760223 · 1976-09-07

ApplicantMediscra, Inc.
Decision Date1976-09-07
Product Code
DecisionSubstantially Equivalent

Device Summary

SCANNER, ULTRASOUND BODY/HEART is the device name listed in this FDA 510(k) record. The listed applicant is Mediscra, Inc.. It received FDA 510(k) clearance on 1976-09-07 under 510(k) number K760223. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANNER, ULTRASOUND BODY/HEART?

SCANNER, ULTRASOUND BODY/HEART is a medical device that received FDA 510(k) clearance on 1976-09-07. The listed applicant is Mediscra, Inc.. The 510(k) number is K760223.

When did SCANNER, ULTRASOUND BODY/HEART receive FDA 510(k) clearance?

SCANNER, ULTRASOUND BODY/HEART received FDA 510(k) clearance on 1976-09-07, under 510(k) number K760223.

Who is the listed applicant for SCANNER, ULTRASOUND BODY/HEART?

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

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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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