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

CCO SYSTEM MODEL SP1467,SP5567,SP6267

K Number: K892941 · Decision Nov 6, 1989
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
36
Applicant Total
13
Review Days
199

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Basic Information

Device Name
CCO SYSTEM MODEL SP1467,SP5567,SP6267
K Number
K892941
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1915
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Spectramed, Inc.
Date Received
April 21, 1989
Decision Date
November 6, 1989
Product Code
KRB
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
KRB Probe, Thermodilution

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Other Clearances by Spectramed, Inc.

K Number Device Name
K896122 AMNICATHDL(TM) DT-IUPC2 DUAL LUMEN TRANS. TIPPED
K895323 MODEL DT-BAL, BALANCE SAVER
K894362 MODEL DT-IUPC2 TRANSDUCER TIPPED DUAL LUMEN IUP
K881857 AMNICATH(TM) MODEL DT-IUPC TRANS. TIPPED INTRAU.
K885235 SAFE-DRAW(TM) BLOOD SAMPLING RESERVOIR & ACCESS.
K881825 MODELS SP5825/SP5835/SP5845/SP5855 PERCU. SHEATH
K875337 HEPARIN COATED LUMINAL PACING CATHETER
K880740 MODEL TA-CS10 SPECTRAJECT CONTROL SYRINGE
K873168 SPECTRAMED DISPOSABLE TRANSDUCER (DT-XXO) & ACCESS
K871573 CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS
Search all 13 clearances from Spectramed, Inc. →