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

INPECTRA STO2 SPOT CHECK

K Number: K103613 · Decision Mar 2, 2011
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
73
Applicant Total
8
Review Days
83

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Basic Information

Device Name
INPECTRA STO2 SPOT CHECK
K Number
K103613
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hutchinson Technology, Inc.
Date Received
December 9, 2010
Decision Date
March 2, 2011
Product Code
MUD
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MUD Oximeter, Tissue Saturation

Similar 510(k) Clearances

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

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Other Clearances by Hutchinson Technology, Inc.

K Number Device Name
K100915 INSPECTRA STO2 TISSUE OXYGENATION MONITOR, MODEL 650
K061619 INSPECTRA STO2 TISSUE OXYGENATION MONITOR
K053618 INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325
K042020 SPECTRA TISSUE SPECTROMETER SYSTEM (INSPECTRA)
K023938 MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325
K012759 INSPECTRA TISSUE SPECTROMETER SYSTEM (INSPECTRA), MODEL 325
K963903 BIOSPECTROMETER-NB OXIMETER IIII