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FDA 510(k)

BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE

K-Number: K991300 · 1999-07-12

ApplicantDhd Healthcare Corp.
Decision Date1999-07-12
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Healthcare Corp.. It received FDA 510(k) clearance on 1999-07-12 under 510(k) number K991300. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE?

BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE is a medical device that received FDA 510(k) clearance on 1999-07-12. The listed applicant is Dhd Healthcare Corp.. The 510(k) number is K991300.

When did BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE receive FDA 510(k) clearance?

BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE received FDA 510(k) clearance on 1999-07-12, under 510(k) number K991300.

Who is the listed applicant for BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE?

The FDA 510(k) record lists Dhd Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE?

The FDA product code for BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE is BWF.

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.

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Other records listing Dhd Healthcare Corp. 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.

K040718TRUSTK002768ACAPELLAK003146CLINIFLO INCENTIVE SPIROMETERK991561ROADRUNNER, PEP THERAPY DEVICEK983467THERAPEPK980662LICHEN, BACTERIAL IN LINE BREATHING FILTER

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Related Devices (Code: BWF)

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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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