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FDA 510(k)

LINEAR SCANNER PROBE, MODEL TL-50

K-Number: K854959 · 1986-06-16

ApplicantElscint, Inc.
Decision Date1986-06-16
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LINEAR SCANNER PROBE, MODEL TL-50 is the device name listed in this FDA 510(k) record. The listed applicant is Elscint, Inc.. It received FDA 510(k) clearance on 1986-06-16 under 510(k) number K854959. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINEAR SCANNER PROBE, MODEL TL-50?

LINEAR SCANNER PROBE, MODEL TL-50 is a medical device that received FDA 510(k) clearance on 1986-06-16. The listed applicant is Elscint, Inc.. The 510(k) number is K854959.

When did LINEAR SCANNER PROBE, MODEL TL-50 receive FDA 510(k) clearance?

LINEAR SCANNER PROBE, MODEL TL-50 received FDA 510(k) clearance on 1986-06-16, under 510(k) number K854959.

Who is the listed applicant for LINEAR SCANNER PROBE, MODEL TL-50?

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 LINEAR SCANNER PROBE, MODEL TL-50?

The FDA product code for LINEAR SCANNER PROBE, MODEL TL-50 is IYO.

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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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