SELECT/SP
K-Number: K961464 · 1996-07-03
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Device Summary
Frequently Asked Questions
What is the SELECT/SP?
SELECT/SP is a medical device that received FDA 510(k) clearance on 1996-07-03. The listed applicant is Elscint, Inc.. The 510(k) number is K961464.
When did SELECT/SP receive FDA 510(k) clearance?
SELECT/SP received FDA 510(k) clearance on 1996-07-03, under 510(k) number K961464.
Who is the listed applicant for SELECT/SP?
The FDA 510(k) record lists Elscint, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SELECT/SP?
The FDA product code for SELECT/SP is JAK.
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 Elscint, 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: JAK)
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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