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

MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325

K Number: K023938 · Decision Dec 13, 2002
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
73
Applicant Total
8
Review Days
17

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Basic Information

Device Name
MODIFICATION TO INSPECTRA TISSUE SPECTROMETER SYSTEM, MODEL 325
K Number
K023938
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hutchinson Technology, Inc.
Date Received
November 26, 2002
Decision Date
December 13, 2002
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

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Other Clearances by Hutchinson Technology, Inc.

K Number Device Name
K103613 INPECTRA STO2 SPOT CHECK
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)
K012759 INSPECTRA TISSUE SPECTROMETER SYSTEM (INSPECTRA), MODEL 325
K963903 BIOSPECTROMETER-NB OXIMETER IIII