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FDA 510(k)

EASYFIT SILKGEL NASAL MASK

K-Number: K110884 · 2011-07-12

Decision Date2011-07-12
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EASYFIT SILKGEL NASAL MASK is the device name listed in this FDA 510(k) record. The listed applicant is Weinmann Gerate Fur Medizin GmbH + Co. KG. It received FDA 510(k) clearance on 2011-07-12 under 510(k) number K110884. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYFIT SILKGEL NASAL MASK?

EASYFIT SILKGEL NASAL MASK is a medical device that received FDA 510(k) clearance on 2011-07-12. The listed applicant is Weinmann Gerate Fur Medizin GmbH + Co. KG. The 510(k) number is K110884.

When did EASYFIT SILKGEL NASAL MASK receive FDA 510(k) clearance?

EASYFIT SILKGEL NASAL MASK received FDA 510(k) clearance on 2011-07-12, under 510(k) number K110884.

Who is the listed applicant for EASYFIT SILKGEL NASAL MASK?

The FDA 510(k) record lists Weinmann Gerate Fur Medizin GmbH + Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EASYFIT SILKGEL NASAL MASK?

The FDA product code for EASYFIT SILKGEL NASAL MASK is BZD.

Related Clinical Trials

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.

Other records listing Weinmann Gerate Fur Medizin GmbH + Co. KG as applicant

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.

View all 9 devices →

Related Devices (Code: BZD)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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