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FDA 510(k)

DEVILBISS MODEL 8500D AND 8500D-608

K-Number: K894244 · 1989-10-06

ApplicantDevilbiss Health Care, Inc.
Decision Date1989-10-06
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DEVILBISS MODEL 8500D AND 8500D-608 is the device name listed in this FDA 510(k) record. The listed applicant is Devilbiss Health Care, Inc.. It received FDA 510(k) clearance on 1989-10-06 under 510(k) number K894244. The device is classified under product code CCQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEVILBISS MODEL 8500D AND 8500D-608?

DEVILBISS MODEL 8500D AND 8500D-608 is a medical device that received FDA 510(k) clearance on 1989-10-06. The listed applicant is Devilbiss Health Care, Inc.. The 510(k) number is K894244.

When did DEVILBISS MODEL 8500D AND 8500D-608 receive FDA 510(k) clearance?

DEVILBISS MODEL 8500D AND 8500D-608 received FDA 510(k) clearance on 1989-10-06, under 510(k) number K894244.

Who is the listed applicant for DEVILBISS MODEL 8500D AND 8500D-608?

The FDA 510(k) record lists Devilbiss Health Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEVILBISS MODEL 8500D AND 8500D-608?

The FDA product code for DEVILBISS MODEL 8500D AND 8500D-608 is CCQ.

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Other records listing Devilbiss Health Care, 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.

K963349DEVILBISS 8650DK970289COMPRESSOR/NEBULIZER #3650K961126PULSE DOSE SERIESK950849MODEL #7354K952491MODEL 7355K952249JET NEBULIZER

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Related Devices (Code: CCQ)

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.

K972397EZ SPRAYIntertex Research, Inc.K964956E-Z SPACER MASK (SMALL)Airpharma, LLCK961894MDI TUTORMdi Tutor, Inc.K961455MEDSHIELD/AEROCHAMBERDiemolding Corp.K960593SMARTMIST ASTHMA MANAGMENT SYSTEM, SMARTMIST, MODEL NUMBER SM-100/SMARTMIST SPIROMETRY AIRWAY, MODEL NUMBER SA-100Aradigm Corp.K922033SALINE SOLUTION- STERILETrinity Laboratories, Inc.

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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