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

PACEVIEW

K Number: K915627 · Decision Mar 27, 1992
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
36
Applicant Total
6
Review Days
109

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Basic Information

Device Name
PACEVIEW
K Number
K915627
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1915
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Micromedical Industries, Ltd.
Date Received
December 9, 1991
Decision Date
March 27, 1992
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 Micromedical Industries, Ltd.

K Number Device Name
K013311 MODIFICATION TO: POCKETVIEW ECG SOFTWARE
K012540 BLY-501 ADAPTOR
K990266 MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE
K922528 CMS SYSTEM
K915624 MODIFIED BIOLOG