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FDA 510(k)

PAPILLON MASK SET

K-Number: K023068 · 2003-05-28

Decision Date2003-05-28
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PAPILLON MASK SET is the device name listed in this FDA 510(k) record. The listed applicant is Map Medizintechnik Fur Arzt Und Patient GmbH. It received FDA 510(k) clearance on 2003-05-28 under 510(k) number K023068. 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 PAPILLON MASK SET?

PAPILLON MASK SET is a medical device that received FDA 510(k) clearance on 2003-05-28. The listed applicant is Map Medizintechnik Fur Arzt Und Patient GmbH. The 510(k) number is K023068.

When did PAPILLON MASK SET receive FDA 510(k) clearance?

PAPILLON MASK SET received FDA 510(k) clearance on 2003-05-28, under 510(k) number K023068.

Who is the listed applicant for PAPILLON MASK SET?

The FDA 510(k) record lists Map Medizintechnik Fur Arzt Und Patient GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAPILLON MASK SET?

The FDA product code for PAPILLON MASK SET 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 Map Medizintechnik Fur Arzt Und Patient GmbH 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.

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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