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FDA 510(k)

DEVILBISS PD1000

K-Number: K020329 · 2002-06-19

ApplicantSunrise Medical Hhg, Inc.
Decision Date2002-06-19
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DEVILBISS PD1000 is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Medical Hhg, Inc.. It received FDA 510(k) clearance on 2002-06-19 under 510(k) number K020329. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEVILBISS PD1000?

DEVILBISS PD1000 is a medical device that received FDA 510(k) clearance on 2002-06-19. The listed applicant is Sunrise Medical Hhg, Inc.. The 510(k) number is K020329.

When did DEVILBISS PD1000 receive FDA 510(k) clearance?

DEVILBISS PD1000 received FDA 510(k) clearance on 2002-06-19, under 510(k) number K020329.

Who is the listed applicant for DEVILBISS PD1000?

The FDA 510(k) record lists Sunrise Medical Hhg, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEVILBISS PD1000?

The FDA product code for DEVILBISS PD1000 is NFB.

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Other records listing Sunrise Medical Hhg, Inc. 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.

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Related Devices (Code: NFB)

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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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