FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DISPOS. MEDICATION NEBULIZER

K Number: K831270 · Decision Jun 8, 1983
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
27
Review Days
50

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DISPOS. MEDICATION NEBULIZER
K Number
K831270
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Hospitak, Inc.
Date Received
April 19, 1983
Decision Date
June 8, 1983
Product Code
CAF
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CAF Nebulizer (Direct Patient Interface)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CAF), ordered by most recent decision date.

View all

Other Clearances by Hospitak, Inc.

K Number Device Name
K955483 TRACH MASK MODEL (245, 246)
K954787 ILLUMINATOR
K953620 WARM N WET HMEF W/LUER ADAPTER
K953619 WARM N WET HME W/LUER ADAPTER
K915750 DISPOSABLE BACTERIAL BREATHNG FILTER
K920842 AEROSOL DELIVERY SYSTEMS
K915228 DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL
K873286 DISPOSABLE, MANUAL PULMONARY RESUSCITATOR
K853600 INFLATABLE AIR SPLINTS
K844328 OXYGEN CONCENTRATOR
Search all 27 clearances from Hospitak, Inc. →