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

DGH-500 PACHYMETER

K Number: K920906 · Decision Nov 2, 1992
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
7
Review Days
249

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Basic Information

Device Name
DGH-500 PACHYMETER
K Number
K920906
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dgh Technology, Inc.
Date Received
February 27, 1992
Decision Date
November 2, 1992
Product Code
IYO
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
IYO System, Imaging, Pulsed Echo, Ultrasonic

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Other Clearances by Dgh Technology, Inc.

K Number Device Name
K171301 Scanmate Flex
K093371 MODEL DGH 6000 SCANMATE A
K033385 DGH 55 HANDHELD PACHYMETER (PACHMATE)
K965127 DGH MODEL 9000
K913067 DGH-4000 A-SCAN/PACHYMETER
K872726 DGH-3000A A-SCAN