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FDA 510(k)

CEILEX LS-15/ALLMEC ARGOSTAT

K-Number: K837352 · 1983-04-13

ApplicantElscint, Inc.
Decision Date1983-04-13
Product Code
DecisionSubstantially Equivalent

Device Summary

CEILEX LS-15/ALLMEC ARGOSTAT is the device name listed in this FDA 510(k) record. The listed applicant is Elscint, Inc.. It received FDA 510(k) clearance on 1983-04-13 under 510(k) number K837352. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEILEX LS-15/ALLMEC ARGOSTAT?

CEILEX LS-15/ALLMEC ARGOSTAT is a medical device that received FDA 510(k) clearance on 1983-04-13. The listed applicant is Elscint, Inc.. The 510(k) number is K837352.

When did CEILEX LS-15/ALLMEC ARGOSTAT receive FDA 510(k) clearance?

CEILEX LS-15/ALLMEC ARGOSTAT received FDA 510(k) clearance on 1983-04-13, under 510(k) number K837352.

Who is the listed applicant for CEILEX LS-15/ALLMEC ARGOSTAT?

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

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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.

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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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