MASKA, OXYGEN VINYL D-SP. SINGLE USE— 510(k) K760219

Name: FDA 510(k) clearance K760219
Creator: U.S. Food and Drug Administration
Published: 1976-08-03

Substantially Equivalent

Manner Medical Products

FDA 510(k) clearance K760219 for MASKA, OXYGEN VINYL D-SP. SINGLE USE, Substantially Equivalent on 1976-08-03. Applicant: Manner Medical Products. Device class: 1.

Clearance details

Applicant: Manner Medical Products
Product code: Code BYG
Device class: Class 1
Regulation: 21 CFR 868.5580
Advisory panel: Anesthesiology
Date received: 1976-07-12
Decision date: 1976-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BYG

view all

K963298 — FIRST AID KIT(S)1996-11-06
K962848 — HANS RUDOLPH NASAL CPAP MASK1996-10-16
K945482 — DISPOSABLE, CPAP OXYGEN MASK1995-09-19
K953464 — WESTMED PEDIATRIC & ADULT MEDIUM CONCENTRATION OXYGEN MASK1995-09-18
K953039 — VARIOUS ADULT & CHILD HIGH CON/NONREBREATH OXY MASKS1995-09-15

More clearances from Manner Medical Products

view all

K760218 — CANNULAE, PLASTIC DISPOSABLE NASAL1976-08-03
K760220 — TUBING, SINGLE USE OXYGEN SUPPLY1976-08-03
K760221 — I.P.P.B., DIS. W/MANIFOLD/NEBULIZER1976-08-03

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