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

MAGELLAN-2200, MODEL-3 ANESTHESIA MACHINE

K Number: K072420 · Decision Jan 22, 2008
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
187
Applicant Total
4
Review Days
147

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
MAGELLAN-2200, MODEL-3 ANESTHESIA MACHINE
K Number
K072420
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.5160
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Oceanic Medical Products, Inc.
Date Received
August 28, 2007
Decision Date
January 22, 2008
Product Code
BSZ
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
BSZ Gas-Machine, Anesthesia

Similar 510(k) Clearances

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

View all

Other Clearances by Oceanic Medical Products, Inc.

K Number Device Name
K060193 MAGELLAN-2200 MODEL -2 ANESTHESIA MACHINE, MODEL 2
K010613 MAGELLAN-2200, MODEL 1
K002951 MAGELLAN VENTILATOR