← Product Code [BTI](/submissions/AN/subpart-g%E2%80%94miscellaneous/BTI) · K963349 # DEVILBISS 8650D (K963349) _Devilbiss Health Care, Inc. · BTI · Jun 13, 1997 · Anesthesiology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/AN/subpart-g%E2%80%94miscellaneous/BTI/K963349 ## Device Facts - **Applicant:** Devilbiss Health Care, Inc. - **Product Code:** [BTI](/submissions/AN/subpart-g%E2%80%94miscellaneous/BTI.md) - **Decision Date:** Jun 13, 1997 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 868.6250 - **Device Class:** Class 2 - **Review Panel:** Anesthesiology - **Attributes:** Therapeutic, Pediatric ## Intended Use The DeVilbiss 8650D is used with a pneumatic nebulizer to administer humidified air or medication into the airways to treat respiratory disorders. The device is intended for home health care and institutional use. Users of this device are adult and pediatric patients with tracheostomies or suffer from asthma, cystic fibrosis, and chronic obstructive pulmonary disease. ## Device Story Portable AC-powered air compressor; provides air source for pneumatic nebulizers. Features metal housing with sound-barrier foam; internal cooling fan for continuous operation. Used in home health care and institutional settings by patients or clinicians. Device delivers humidified air or aerosolized medication to airways; supports respiratory therapy for asthma, cystic fibrosis, COPD, and tracheostomy care. Clinical benefit: effective delivery of prescribed respiratory treatments. ## Clinical Evidence Bench testing only. Testing included pressure and flow output, sound pressure level, temperature rise, shipping performance, and electromagnetic compatibility. No clinical data provided. ## Technological Characteristics AC-powered air compressor; metal housing with sound-barrier foam; internal cooling fan. Meets UL-544 standard for medical/dental equipment. Standalone device. ## Regulatory Identification A portable air compressor is a device intended to provide compressed air for medical purposes, e.g., to drive ventilators and other respiratory devices. ## Special Controls *Classification.* Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 868.9. ## Predicate Devices - Allied Healthcare/Timeter PCS414 ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0} 13 koi K963349 # 510(k) SUMMARY STATEMENT Submitter: DeVilbiss Health Care, Inc. 1200 East Main Street P.O. Box 635 Somerset, Pa 15501-0635 USA Contact: Matt Smith 814-443-7531 814-443-7571 FAX Date of 510(k) Submittal: August 26, 1996 Classification Name: Pump, Nebulizer, Electrically Powered Common Name: Compressor used for nebulization and humidification Proprietary Name: 8650D Equivalent to Device: Allied Healthcare/Timeter PCS414 ## Description of Device: The DeVilbiss 8650D Compressor is a portable AC powered air compressor that will act as an air source to operate a pneumatic nebulizer. The device has an internal cooling fan to allow continuous use operation. It uses a metal housing with sound barrier foam to provide a low noise level. ## Intended Use of Device: The DeVilbiss 8650D is used with a pneumatic nebulizer to administer humidified air or medication into the airways to treat respiratory disorders. The device is intended for home health care and institutional use. Users of this device are adult and pediatric patients with tracheostomies or suffer from asthma, cystic fibrosis, and chronic obstructive pulmonary disease. ## Performance Testing: The DeVilbiss 8650D was tested for pressure and flow output, sound pressure level, temperature rise, and shipping performance. and electromagnetic compatibility. ## Agency Approvals: The DeVilbiss 8650D will meet UL-544 Standard for Safety, Medical and Dental Equipment. ## Conclusion: The results of the above testing do not indicate any safety and effectiveness concerns as compared to the Allied Healthcare PCS 414. {1} DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 JUN 13 1997 Mr. Matt Smith DeVilbiss Health Care, Inc. 1200 East Main Street P.O. Box 635 Somerset, Pennsylvania 15501-0635 Re: *K963349 DeVilbiss 8650D Regulatory Class: II (two) Product Code: 73 BTI Dated: May 18, 1997 Received: May 19, 1997 Dear Mr. Smith: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) regulation (21 CFR Part 820) and that, through periodic GMP inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations. {2} Page 2 - Mr. Matt Smith This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for *in vitro* diagnostic devices), please contact the Office of Compliance at (301) 594-4646. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html". Sincerely yours, ![img-0.jpeg](img-0.jpeg) Thomas J. Callahan, Ph.D. Director Division of Cardiovascular, Respiratory, and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {3} K963349/A Page 1 of 1 510(k) Number (if known): K963349 Device Name: DeVilbiss Health Care, Inc. 8650D Compressor Indications For Use: The 8650D will be used as the air source to nebulize sterile water to provide humidification to patients with tracheostomies. The 8650D may also be used to nebulize medications in the treatment of Asthma, Cystic Fibrosis, and chronic obstructive pulmonary disease. (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Curtis D. Truesdale (Division Sign-Off) Division of Cardiovascular, Respiratory, and Neurological Devices 510(k) Number K963349 Prescription Use ☑ (Per 21 CFR 801.109) OR Over-The-Counter Use ☐ (Optional Format 1-2-96) --- **Source:** [https://fda.innolitics.com/submissions/AN/subpart-g%E2%80%94miscellaneous/BTI/K963349](https://fda.innolitics.com/submissions/AN/subpart-g%E2%80%94miscellaneous/BTI/K963349) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. 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