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

ROLLER ELECTRODE

K Number: K954488 · Decision Mar 6, 1997
Classifications
1
FEI Numbers
135
Registration Numbers
135
Same Product Code
170
Applicant Total
149
Review Days
526

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Basic Information

Device Name
ROLLER ELECTRODE
K Number
K954488
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1690
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Olympus America, Inc.
Date Received
September 27, 1995
Decision Date
March 6, 1997
Product Code
HIH
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HIH Hysteroscope (And Accessories)

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Other Clearances by Olympus America, Inc.

K Number Device Name
K111788 ENDOEYE HD II
K081615 OLYMPUS CEA - CARCINOEMBRYONIC ANTIGEN
K073487 OLYMPUS IGM REAGENT
K073490 OLYMPUS IGG REAGENT
K073489 OLYMPUS IGA REAGENT
K062862 OLYMPUS URIC ACID REAGENT, MODEL OSR6X98
K063804 OLYMPUS TRIGLYCERIDE TEST SYSTEM
K061499 OSFERION
K062581 OLYMPUS TSH REAGENT, CALIBRATOR AND CONTROL AND AU3000I IMMUNOASSAY SYSTEM
K061575 OLYMPUS CALCIUM ARSENAZO REAGENT, OSR60117, OSR61117, OSR65117
Search all 149 clearances from Olympus America, Inc. →