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FDA 510(k)

CONDOR ULTRASONIC INSERTS

K-Number: K943403 · 1996-03-05

ApplicantCondor Products, Inc.
Decision Date1996-03-05
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CONDOR ULTRASONIC INSERTS is the device name listed in this FDA 510(k) record. The listed applicant is Condor Products, Inc.. It received FDA 510(k) clearance on 1996-03-05 under 510(k) number K943403. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONDOR ULTRASONIC INSERTS?

CONDOR ULTRASONIC INSERTS is a medical device that received FDA 510(k) clearance on 1996-03-05. The listed applicant is Condor Products, Inc.. The 510(k) number is K943403.

When did CONDOR ULTRASONIC INSERTS receive FDA 510(k) clearance?

CONDOR ULTRASONIC INSERTS received FDA 510(k) clearance on 1996-03-05, under 510(k) number K943403.

Who is the listed applicant for CONDOR ULTRASONIC INSERTS?

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

What is the FDA product code for CONDOR ULTRASONIC INSERTS?

The FDA product code for CONDOR ULTRASONIC INSERTS is ELC.

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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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