FDA 510(k) Substantially Equivalent 🇺🇸 United States

MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT

K Number: K974087 · Decision Jun 15, 1998
Classifications
0
FEI Numbers
11
Registration Numbers
11
Same Product Code
82
Applicant Total
230
Review Days
229

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Basic Information

Device Name
MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT
K Number
K974087
Clearance Type
Traditional
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hewlett-Packard Co.
Date Received
October 29, 1997
Decision Date
June 15, 1998
Product Code
LOS
Advisory Committee
Unknown
Review Advisory Committee
CV
Third Party
N

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