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FDA 510(k)

SELECT/SP

K-Number: K961464 · 1996-07-03

ApplicantElscint, Inc.
Decision Date1996-07-03
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SELECT/SP is the device name listed in this FDA 510(k) record. The listed applicant is Elscint, Inc.. It received FDA 510(k) clearance on 1996-07-03 under 510(k) number K961464. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 94 devices →

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

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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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