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FDA 510(k)

SINVISION 2001 ULTRASOUND SCANNER

K-Number: K802484 · 1980-12-01

ApplicantNational Ultrasound Corp.
Decision Date1980-12-01
Product Code
DecisionSubstantially Equivalent

Device Summary

SINVISION 2001 ULTRASOUND SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is National Ultrasound Corp.. It received FDA 510(k) clearance on 1980-12-01 under 510(k) number K802484. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINVISION 2001 ULTRASOUND SCANNER?

SINVISION 2001 ULTRASOUND SCANNER is a medical device that received FDA 510(k) clearance on 1980-12-01. The listed applicant is National Ultrasound Corp.. The 510(k) number is K802484.

When did SINVISION 2001 ULTRASOUND SCANNER receive FDA 510(k) clearance?

SINVISION 2001 ULTRASOUND SCANNER received FDA 510(k) clearance on 1980-12-01, under 510(k) number K802484.

Who is the listed applicant for SINVISION 2001 ULTRASOUND SCANNER?

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

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 National Ultrasound Corp. 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.

K812588SCANNER 700

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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