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

GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR

K Number: K902906 · Decision Oct 15, 1990
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
7
Applicant Total
2
Review Days
104

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
GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR
K Number
K902906
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6100
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Gas-Vak
Date Received
July 3, 1990
Decision Date
October 15, 1990
Product Code
FLI
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FLI Cabinet, Ethylene-Oxide Gas Aerator

Similar 510(k) Clearances

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

View all

Other Clearances by Gas-Vak

K Number Device Name
K890438 GAS-VAK(R), MODEL 300