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FDA 510(k)

SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER

K-Number: K880900 · 1988-06-01

Decision Date1988-06-01
Product CodeHEM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Corometrics Medical Systems, Inc.. It received FDA 510(k) clearance on 1988-06-01 under 510(k) number K880900. The device is classified under product code HEM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER?

SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER is a medical device that received FDA 510(k) clearance on 1988-06-01. The listed applicant is Corometrics Medical Systems, Inc.. The 510(k) number is K880900.

When did SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER receive FDA 510(k) clearance?

SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER received FDA 510(k) clearance on 1988-06-01, under 510(k) number K880900.

Who is the listed applicant for SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER?

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

What is the FDA product code for SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER?

The FDA product code for SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER is HEM.

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.

Other records listing Corometrics Medical Systems, Inc. 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.

Related Devices (Code: HEM)

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.

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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