The Devilbiss Co.
The Devilbiss Co. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1987.
Top product codes for The Devilbiss Co.
Recent clearances by The Devilbiss Co.
- K874041 — DEVILBISS MODEL 8500D
- K872094 — VACU-AIDE
- K872826 — ULTRA-NEB 99 ULTRASONIC NEBULIZER
- K872470 — DEVO/MC44 OXYGEN CONCENTRATOR
- K854520 — PULMO-AIDE MODEL 5610D
- K852209 — DEVO/MC29 OXYGEN CONCENTRATOR MC29D
- K851695 — ULTRA-NEB 100 ULTRASONIC NEBULIZER
- K830174 — DE VO/44 OXYGEN CONCENTRATOR #444
- K801526 — SURVEYOR I, RESPIRATORY COMPUTER SYSTEM
- K792385 — DEVO OXYGEN CONCENTRATOR, MODEL 955
- K781073 — PULMO-SONIC
- K770157 — DEVILBISS OXYGEN ENRICHER
Data sourced from openFDA. This site is unofficial and independent of the FDA.