FDA 510(k)

INSIGHT ELECTRONIC ALIGNMENT INDICATOR

K-Number: K940812 · 1994-11-21

Decision Date1994-11-21

Product CodeKQX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

INSIGHT ELECTRONIC ALIGNMENT INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Andronic Devices, Ltd.. It received FDA 510(k) clearance on 1994-11-21 under 510(k) number K940812. The device is classified under product code KQX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSIGHT ELECTRONIC ALIGNMENT INDICATOR?

INSIGHT ELECTRONIC ALIGNMENT INDICATOR is a medical device that received FDA 510(k) clearance on 1994-11-21. The listed applicant is Andronic Devices, Ltd.. The 510(k) number is K940812.

When did INSIGHT ELECTRONIC ALIGNMENT INDICATOR receive FDA 510(k) clearance?

INSIGHT ELECTRONIC ALIGNMENT INDICATOR received FDA 510(k) clearance on 1994-11-21, under 510(k) number K940812.

Who is the listed applicant for INSIGHT ELECTRONIC ALIGNMENT INDICATOR?

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

What is the FDA product code for INSIGHT ELECTRONIC ALIGNMENT INDICATOR?

The FDA product code for INSIGHT ELECTRONIC ALIGNMENT INDICATOR is KQX.

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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.