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

GLASS MERCURY FILLED THERMOMETERS

K Number: K893602 · Decision Aug 8, 1989
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
32
Applicant Total
34
Review Days
85

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Basic Information

Device Name
GLASS MERCURY FILLED THERMOMETERS
K Number
K893602
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2920
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Smith & Nephew United, Inc.
Date Received
May 15, 1989
Decision Date
August 8, 1989
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

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Other Clearances by Smith & Nephew United, Inc.

K Number Device Name
K963096 ALLEVYN HYDRO POLY DRESSING ND ALL TRAC DRESSING
K961775 PROFORE FOUR-LAYER BANDAGE SYSTEM KIT
K945330 ALLEVYN ADHESIVE
K943619 CAVI-CARE CONFORMING FOAM DRESSING
K942748 INTRASITE
K935705 ALLEVYN ISLAND WOUND DRESSING
K935803 CICA-CARE SILICONE GEL SHEET
K932263 SOLOSITE DERMAL WOUND GEL
K926508 INTRASITE GEL
K922897 STRAPPAL
Search all 34 clearances from Smith & Nephew United, Inc. →