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FDA 510(k)

FX-CABLELOK SYSTEM, MODIFICATION

K-Number: K915259 · 1992-02-07

ApplicantBiodynamic Technologies, Inc.
Decision Date1992-02-07
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FX-CABLELOK SYSTEM, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Biodynamic Technologies, Inc.. It received FDA 510(k) clearance on 1992-02-07 under 510(k) number K915259. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FX-CABLELOK SYSTEM, MODIFICATION?

FX-CABLELOK SYSTEM, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-02-07. The listed applicant is Biodynamic Technologies, Inc.. The 510(k) number is K915259.

When did FX-CABLELOK SYSTEM, MODIFICATION receive FDA 510(k) clearance?

FX-CABLELOK SYSTEM, MODIFICATION received FDA 510(k) clearance on 1992-02-07, under 510(k) number K915259.

Who is the listed applicant for FX-CABLELOK SYSTEM, MODIFICATION?

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

What is the FDA product code for FX-CABLELOK SYSTEM, MODIFICATION?

The FDA product code for FX-CABLELOK SYSTEM, MODIFICATION is JDQ.

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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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