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

CRM-114 COLOR VIDEO CAMERA

K Number: K830924 · Decision Apr 18, 1983
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
97
Applicant Total
4
Review Days
27

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Basic Information

Device Name
CRM-114 COLOR VIDEO CAMERA
K Number
K830924
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Umi, Inc.
Date Received
March 22, 1983
Decision Date
April 18, 1983
Product Code
FET
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology

Similar 510(k) Clearances

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

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Other Clearances by Umi, Inc.

K Number Device Name
K883527 GRID/RADIOGRAPHIC
K831412 CRM-100 COLOR VIDEO CAMERA
K823382 NEPHROSTOMY CATHETER