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

CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100

K Number: K992606 · Decision Jun 21, 2000
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
86
Applicant Total
48
Review Days
323

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
CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100
K Number
K992606
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Canon USA, Inc.
Date Received
August 3, 1999
Decision Date
June 21, 2000
Product Code
HLI
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HLI Ophthalmoscope, Ac-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Canon USA, Inc.

K Number Device Name
K090623 DIGITAL RADIOGRAPHY CXDI-40G COMPACT
K033624 PACS SOFTWARE SOLUTION 2003
K031633 CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C
K031629 CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI
K023750 CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G
K023586 DR-ER VERFSION OF CANON X-RAY DIGITAL CAMERAS
K003689 CANON X-RAY DIGITAL CAMERA, MODEL CXDI-31
K992547 CANON X-RAY DIGITAL CAMERA, MODEL CXDI-22
K981556 CANON X-RAY DIGITAL CAMERA CXDI-11
K980246 NON-MYDRIATIC RETINAL CAMERA, MODEL CR6-45NM
Search all 48 clearances from Canon USA, Inc. →