FDA 510(k)

SCANNER 560 ULTRASOUND SCANNER

K-Number: K827713 · 1982-08-10

Decision Date1982-08-10

Product Code

DecisionSubstantially Equivalent

Device Summary

SCANNER 560 ULTRASOUND SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Pie Data, Inc.. It received FDA 510(k) clearance on 1982-08-10 under 510(k) number K827713. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANNER 560 ULTRASOUND SCANNER?

SCANNER 560 ULTRASOUND SCANNER is a medical device that received FDA 510(k) clearance on 1982-08-10. The listed applicant is Pie Data, Inc.. The 510(k) number is K827713.

When did SCANNER 560 ULTRASOUND SCANNER receive FDA 510(k) clearance?

SCANNER 560 ULTRASOUND SCANNER received FDA 510(k) clearance on 1982-08-10, under 510(k) number K827713.

Who is the listed applicant for SCANNER 560 ULTRASOUND SCANNER?

The FDA 510(k) record lists Pie Data, Inc. 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 Pie Data, Inc. as applicant

K828621VIDEO IMAGE PROCESSOR

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.