RESPIRATORY EXERCISOR, VOLUME PULSE— 510(k) K781669

Name: FDA 510(k) clearance K781669
Creator: U.S. Food and Drug Administration
Published: 1978-10-23

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K781669 for RESPIRATORY EXERCISOR, VOLUME PULSE, Substantially Equivalent on 1978-10-23. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code BWF
Device class: Class 2
Regulation: 21 CFR 868.5690
Advisory panel: Anesthesiology
Date received: 1978-10-03
Decision date: 1978-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BWF

view all

K241152 — InSee2025-08-21
K233855 — AllPEP2024-02-02
K221058 — LungTrainer (MD2 & MD3)2023-07-05
K222018 — Breathe+2023-06-02
K220565 — Hudson RCI Triflo II Incentive Deep Breathing Exerciser2022-10-25

More clearances from Bd Becton Dickinson Vacutainer Systems Preanalytic

view all

K003062 — BACTEC MGIT 960 SIR KITS2001-06-06
K003553 — 0.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE2001-03-21
K003461 — BD VACUTAINER PASSIVE SHIELDING BLOOD COLLECTION NEEDLE2001-02-01
K002938 — B-D ULTRA-FINE III PEN NEEDLE; MODEL 31G X 3/162000-11-29
K001364 — BD DIRECTIGEN FLU A+B2000-06-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.