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FDA 510(k)

NOBELPHARMA TORQUE CONTROLLER

K-Number: K922805 · 1993-07-22

ApplicantNobelpharma USA, Inc.
Decision Date1993-07-22
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NOBELPHARMA TORQUE CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Nobelpharma USA, Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K922805. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOBELPHARMA TORQUE CONTROLLER?

NOBELPHARMA TORQUE CONTROLLER is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K922805.

When did NOBELPHARMA TORQUE CONTROLLER receive FDA 510(k) clearance?

NOBELPHARMA TORQUE CONTROLLER received FDA 510(k) clearance on 1993-07-22, under 510(k) number K922805.

Who is the listed applicant for NOBELPHARMA TORQUE CONTROLLER?

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

What is the FDA product code for NOBELPHARMA TORQUE CONTROLLER?

The FDA product code for NOBELPHARMA TORQUE CONTROLLER is DZE.

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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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