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

SEARLE NEONATAL OXYGEN PROBE

K Number: K780850 · Decision Aug 23, 1978
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
22
Applicant Total
14
Review Days
93

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Basic Information

Device Name
SEARLE NEONATAL OXYGEN PROBE
K Number
K780850
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1200
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Will Ross Co.
Date Received
May 22, 1978
Decision Date
August 23, 1978
Product Code
CCE
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
CCE Analyzer, Gas, Oxygen, Partial Pressure, Blood-Phase, Indwelling

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K770611 PARALLEL BARS
K770612 SPLINT, BOHLER
K770607 TRACTION HARNESS
K770608 WALKING AID
K770610 TABLE, TREATMENT & TRACTION, HI-LO
K770609 TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT
K770509 TABLE, MASSAGE AND TREATMENT
K770399 VALVE FOR CLOSED SYS. URINARY DRAINAGE
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