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

BUNN MICRO OXYGEN CONCENTRATOR

K Number: K833495 · Decision Nov 29, 1983
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
286
Applicant Total
4
Review Days
53

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Basic Information

Device Name
BUNN MICRO OXYGEN CONCENTRATOR
K Number
K833495
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5440
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Greene & Kellogg, Inc.
Date Received
October 7, 1983
Decision Date
November 29, 1983
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

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Other Clearances by Greene & Kellogg, Inc.

K Number Device Name
K830046 MODEL HI-FLO2 OXYGEN RICH AIR SUPPLY
K811155 MODEL RXO2 OXYGEN RICH AIR SUPPLY
K800534 MODEL 52 BUNN DRY AIR SUPPLY