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

ABCO EXAMINATION LAMP (GOOSENECK TYPE)

K Number: K800230 · Decision Feb 26, 1980
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
36
Applicant Total
127
Review Days
21

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Basic Information

Device Name
ABCO EXAMINATION LAMP (GOOSENECK TYPE)
K Number
K800230
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6320
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Abco Dealers, Inc.
Date Received
February 5, 1980
Decision Date
February 26, 1980
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

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Other Clearances by Abco Dealers, Inc.

K Number Device Name
K905025 DIGITAL THERMOMETER KITS
K882304 DIGITAL THERMOMETER SHEATHS (ORAL AND RECTAL)
K880892 BLOOD COLLECTING NEEDLE AND HOLDERS
K880894 ALLERGIST SYRINGES
K872875 STRETCH GAUZE BANDAGES
K872874 MICROSCOPE COVER GLASSES
K872797 NON-SKID SHOE COVERS
K871465 THERMOMETER SHEATHS
K862726 DISPOSABLE SHOE COVERS AND NURSES CAPS
K862111 ARMBOARDS, REUSABLE AND DISPOSABLE
Search all 127 clearances from Abco Dealers, Inc. →