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

OXYMATIC-24

K Number: K884562 · Decision Jan 9, 1989
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
70
Applicant Total
17
Review Days
70

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
OXYMATIC-24
K Number
K884562
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Chad Therapeutics, Inc.
Date Received
October 31, 1988
Decision Date
January 9, 1989
Product Code
NFB
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
NFB Conserver, Oxygen

Similar 510(k) Clearances

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

View all

Other Clearances by Chad Therapeutics, Inc.

K Number Device Name
K081176 FLOCHANNEL
K070740 CHAD THERAPEUTICS BONSAI MODEL 800
K042142 CHAD THERAPEUTICS LOTUS, MODELS OM-700 AND OM-700S
K033364 CHAD THERAPEUTICS SAGE
K020475 CHAD THERAPEUTICS OXYPENUMATIC CYPRESS MODEL 511
K013472 TOTAL O2
K010389 CHAD THERAPEUTICS OXYMATIC MODEL 401 AND OXYMATIC MODEL 411
K003455 MODIFICATION TO CHAD THERAPEUTICS OXYMATIC MODEL 401
K000890 CHAD THERAPEUTICS OXYMATIC MODEL 401
K971889 CHAD TOTAL O2 DELIVERY SYSTEM
Search all 17 clearances from Chad Therapeutics, Inc. →