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

THERMOMETERS

K Number: K813424 · Decision Dec 18, 1981
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
32
Applicant Total
127
Review Days
11

Basic Information

Device Name
THERMOMETERS
K Number
K813424
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2920
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
ABCO DEALERS, INC.
Date Received
December 7, 1981
Decision Date
December 18, 1981
Product Code
FLK
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
FLK Thermometer, Clinical Mercury

Similar 510(k) Clearances

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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. →