FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

EPISCOPE, MODEL 47300

K Number: K920103 · Decision Apr 28, 1992
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
36
Applicant Total
111
Review Days
110

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EPISCOPE, MODEL 47300
K Number
K920103
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6320
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Welch Allyn, Inc.
Date Received
January 9, 1992
Decision Date
April 28, 1992
Product Code
KZF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KZF Device, Medical Examination, Ac Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KZF), ordered by most recent decision date.

View all

Other Clearances by Welch Allyn, Inc.

K Number Device Name
K243598 Welch Allyn Connex® 360 (Multiple)
K241411 Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM)
K223381 iExaminer System with Panoptic Plus
K212473 Welch Allyn Connex Central Station
K191013 Welch Allyn Diagnostic Cardiology Suite 2.X.X with Spirometry option
K181016 Welch Allyn RetinaVue Network REF 901108 PACS Medical Image System
K171621 Welch Allyn Connex Vital Signs Monitor, Welch Allyn Connex Integrated Wall System, 901060 Vital Signs Monitor
K142356 Connex Spot Monitor,901058 Vital Signs Monitor Core
K132807 MONITORING STATION, CONNEX(R) CENTRAL STATION (CS)
K132808 VITAL SIGNS MONITOR, CONNEX VITAL SIGNS MONITOR
Search all 111 clearances from Welch Allyn, Inc. →