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FDA 510(k)

NORTA

K-Number: K935630 · 1994-10-07

ApplicantBeiersdorf, Inc.
Decision Date1994-10-07
Product CodeEZL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NORTA is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1994-10-07 under 510(k) number K935630. The device is classified under product code EZL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORTA?

NORTA is a medical device that received FDA 510(k) clearance on 1994-10-07. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K935630.

When did NORTA receive FDA 510(k) clearance?

NORTA received FDA 510(k) clearance on 1994-10-07, under 510(k) number K935630.

Who is the listed applicant for NORTA?

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

What is the FDA product code for NORTA?

The FDA product code for NORTA is EZL.

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Other records listing Beiersdorf, Inc. as applicant

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Related Devices (Code: EZL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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