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

OXYGEN/STERILE AIR GEN SYST/SURGICAL HANDPIECES

K Number: K873284 · Decision Nov 16, 1987
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
286
Applicant Total
4
Review Days
91

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Basic Information

Device Name
OXYGEN/STERILE AIR GEN SYST/SURGICAL HANDPIECES
K Number
K873284
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5440
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Litton Systems, Inc.
Date Received
August 17, 1987
Decision Date
November 16, 1987
Product Code
CAW
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
CAW Generator, Oxygen, Portable

Similar 510(k) Clearances

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Other Clearances by Litton Systems, Inc.

K Number Device Name
K013223 PATIENT VENTILATION OXYGEN CONCENTRATING SYSTEM (PVOCS)
K951143 PULSE KLYSTRON AMPLIFIFER (L-5822-90)
K951142 PULSE KLYSTRON AMPLIFIER (L-5822-00)