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FDA 510(k)

DR. THEISS ALERGOL POLLEN BLOCKER CREAM

K-Number: K042610 · 2005-05-16

ApplicantDr. Theiss Naturwaren GmbH
Decision Date2005-05-16
Product CodeNUP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DR. THEISS ALERGOL POLLEN BLOCKER CREAM is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Theiss Naturwaren GmbH. It received FDA 510(k) clearance on 2005-05-16 under 510(k) number K042610. The device is classified under product code NUP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DR. THEISS ALERGOL POLLEN BLOCKER CREAM?

DR. THEISS ALERGOL POLLEN BLOCKER CREAM is a medical device that received FDA 510(k) clearance on 2005-05-16. The listed applicant is Dr. Theiss Naturwaren GmbH. The 510(k) number is K042610.

When did DR. THEISS ALERGOL POLLEN BLOCKER CREAM receive FDA 510(k) clearance?

DR. THEISS ALERGOL POLLEN BLOCKER CREAM received FDA 510(k) clearance on 2005-05-16, under 510(k) number K042610.

Who is the listed applicant for DR. THEISS ALERGOL POLLEN BLOCKER CREAM?

The FDA 510(k) record lists Dr. Theiss Naturwaren GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DR. THEISS ALERGOL POLLEN BLOCKER CREAM?

The FDA product code for DR. THEISS ALERGOL POLLEN BLOCKER CREAM is NUP.

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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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