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FDA 510(k)

BRANEMARK SYSTEM ESTHETICONE NON-ROTATIONAL SYSTEM

K-Number: K934827 · 1994-08-08

ApplicantNobelpharma USA, Inc.
Decision Date1994-08-08
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BRANEMARK SYSTEM ESTHETICONE NON-ROTATIONAL SYSTEM 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 1994-08-08 under 510(k) number K934827. 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 BRANEMARK SYSTEM ESTHETICONE NON-ROTATIONAL SYSTEM?

BRANEMARK SYSTEM ESTHETICONE NON-ROTATIONAL SYSTEM is a medical device that received FDA 510(k) clearance on 1994-08-08. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K934827.

When did BRANEMARK SYSTEM ESTHETICONE NON-ROTATIONAL SYSTEM receive FDA 510(k) clearance?

BRANEMARK SYSTEM ESTHETICONE NON-ROTATIONAL SYSTEM received FDA 510(k) clearance on 1994-08-08, under 510(k) number K934827.

Who is the listed applicant for BRANEMARK SYSTEM ESTHETICONE NON-ROTATIONAL SYSTEM?

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 BRANEMARK SYSTEM ESTHETICONE NON-ROTATIONAL SYSTEM?

The FDA product code for BRANEMARK SYSTEM ESTHETICONE NON-ROTATIONAL SYSTEM is DZE.

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Other records listing Nobelpharma USA, Inc. as applicant

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Related Devices (Code: 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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