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FDA 510(k)

SNIFF POSITION PILLOWS/POPITZ PILLOWS

K-Number: K023010 · 2002-10-01

ApplicantAeolus International Corporation
Decision Date2002-10-01
Product CodeMYB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SNIFF POSITION PILLOWS/POPITZ PILLOWS is the device name listed in this FDA 510(k) record. The listed applicant is Aeolus International Corporation. It received FDA 510(k) clearance on 2002-10-01 under 510(k) number K023010. The device is classified under product code MYB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNIFF POSITION PILLOWS/POPITZ PILLOWS?

SNIFF POSITION PILLOWS/POPITZ PILLOWS is a medical device that received FDA 510(k) clearance on 2002-10-01. The listed applicant is Aeolus International Corporation. The 510(k) number is K023010.

When did SNIFF POSITION PILLOWS/POPITZ PILLOWS receive FDA 510(k) clearance?

SNIFF POSITION PILLOWS/POPITZ PILLOWS received FDA 510(k) clearance on 2002-10-01, under 510(k) number K023010.

Who is the listed applicant for SNIFF POSITION PILLOWS/POPITZ PILLOWS?

The FDA 510(k) record lists Aeolus International Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNIFF POSITION PILLOWS/POPITZ PILLOWS?

The FDA product code for SNIFF POSITION PILLOWS/POPITZ PILLOWS is MYB.

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Related Devices (Code: MYB)

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

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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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