FDA 510(k)

ABC BRAND

K-Number: K823793 · 1983-01-14

Decision Date1983-01-14

Product Code

DecisionSubstantially Equivalent

Device Summary

ABC BRAND is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1983-01-14 under 510(k) number K823793. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABC BRAND?

ABC BRAND is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K823793.

When did ABC BRAND receive FDA 510(k) clearance?

ABC BRAND received FDA 510(k) clearance on 1983-01-14, under 510(k) number K823793.

Who is the listed applicant for ABC BRAND?

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

Related Clinical Trials

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Other records listing Beiersdorf, Inc. as applicant

K090921ANTI-EMBOLISM STOCKINGS, MODELS 71055-00000-02, 71057-00000-02, 71059-00000-02, 71064-00000-02 & 71065-00000-02 K024057CURAD SCAR THERAPY K952526CUTINOVA CAVITY K943363CUTIPLAST STERIL K944581CUTINOVA THIN WOUND DRESSING K935630NORTA

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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.