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

DISKCAM DC 6001

K Number: K884148 · Decision Nov 23, 1988
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
54
Applicant Total
16
Review Days
51

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Basic Information

Device Name
DISKCAM DC 6001
K Number
K884148
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.2010
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Camtronics, Ltd.
Date Received
October 3, 1988
Decision Date
November 23, 1988
Product Code
LMB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LMB Device, Digital Image Storage, Radiological

Similar 510(k) Clearances

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Other Clearances by Camtronics, Ltd.

K Number Device Name
K021236 SURGERY AND ACCESSORIES
K013032 PHYSIOLOG, SERIES 95000
K992666 VIDEO PLUS SYSTEM, SERIES 95000
K992259 ECHOCARDIOGRAPHY SYSTEM SERIES 95000
K990066 CCD CAMERA, MODEL 9000
K955519 ANALYTICAL REVIEW STATION
K954159 DIGITAL IMAGING SYSTEM
K955232 NT SERIES DIGITAL IMAGE MANAGER
K953080 DIGITAL IMAGING SYSTEM INTERFACE
K945654 NICOM DIGITAL IMAGE MANAGER
Search all 16 clearances from Camtronics, Ltd. →