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FDA 510(k)

BALL ATTACHMENT SYSTEM

K-Number: K955372 · 1996-01-23

ApplicantNobelpharma USA, Inc.
Decision Date1996-01-23
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BALL ATTACHMENT 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 1996-01-23 under 510(k) number K955372. 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 BALL ATTACHMENT SYSTEM?

BALL ATTACHMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1996-01-23. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K955372.

When did BALL ATTACHMENT SYSTEM receive FDA 510(k) clearance?

BALL ATTACHMENT SYSTEM received FDA 510(k) clearance on 1996-01-23, under 510(k) number K955372.

Who is the listed applicant for BALL ATTACHMENT 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 BALL ATTACHMENT SYSTEM?

The FDA product code for BALL ATTACHMENT 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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