SSD-620 LINEAR/CONVEX ARRAY SECTOR SCANNER
K-Number: K880900 · 1988-06-01
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Device Summary
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
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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