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FDA 510(k)

DIGITILT LS-30 REMOTE CONTROL

K-Number: K834288 · 1983-12-29

ApplicantElscint, Inc.
Decision Date1983-12-29
Product CodeIZF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITILT LS-30 REMOTE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Elscint, Inc.. It received FDA 510(k) clearance on 1983-12-29 under 510(k) number K834288. The device is classified under product code IZF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITILT LS-30 REMOTE CONTROL?

DIGITILT LS-30 REMOTE CONTROL is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is Elscint, Inc.. The 510(k) number is K834288.

When did DIGITILT LS-30 REMOTE CONTROL receive FDA 510(k) clearance?

DIGITILT LS-30 REMOTE CONTROL received FDA 510(k) clearance on 1983-12-29, under 510(k) number K834288.

Who is the listed applicant for DIGITILT LS-30 REMOTE CONTROL?

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 DIGITILT LS-30 REMOTE CONTROL?

The FDA product code for DIGITILT LS-30 REMOTE CONTROL is IZF.

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Related Devices (Code: IZF)

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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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