EMERSON MODEL 3MV-AP AND 3V-AP PRESS-— 510(k) K832271

Name: FDA 510(k) clearance K832271
Creator: U.S. Food and Drug Administration
Published: 1983-09-12

Substantially Equivalent

J. H. Emerson Co.

FDA 510(k) clearance K832271 for EMERSON MODEL 3MV-AP AND 3V-AP PRESS-, Substantially Equivalent on 1983-09-12. Applicant: J. H. Emerson Co.. Device class: 2.

Clearance details

Applicant: J. H. Emerson Co.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1983-07-12
Decision date: 1983-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAP

view all

K201666 — SINGLE USE MANOMETER2020-11-13
K182292 — VORTRAN APM-Plus2019-09-18
K180510 — NS 120P-TRS Airway Pressure Gauge2019-05-01
K172284 — NAPA LP-15 Airway Pressure Monitor2018-02-09
K153733 — VORTRAN Manometer2016-09-16

More clearances from J. H. Emerson Co.

view all

K002598 — EMERSON COUGH ASSIST MODEL CA-3000 W/AUTOMATIC TIMING AND MODEL CM-3000 W/MANUAL TIMING2000-11-22
K920910 — OXYGEN POWERED RESUSCITATOR FOR CPR1993-01-12
K924174 — EMERSON IN-EXSUFFLATOR, MODELS 2-CM & 2-CA1992-11-17
K902764 — EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM1990-11-19
K896721 — MODEL 7-AT TREATMENT CHAMBER1990-01-22

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