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

TEK-LUBE

K Number: K925080 · Decision Jan 31, 1994
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
260
Applicant Total
12
Review Days
481

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Basic Information

Device Name
TEK-LUBE
K Number
K925080
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Clinical Technology Corp.
Date Received
October 7, 1992
Decision Date
January 31, 1994
Product Code
EFB
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EFB Handpiece, Air-Powered, Dental

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K855138 BOVIE ULTRASONIC SURGICAL SYSTEM
K854231 ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES
K853507 STERI-GRIP
K852986 GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN
K844565 BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT)
K841272 SICKLE-STAT HEMOGLOBIN S SCREEN KIT
K823077 URINARY BLADDER TEMP. SENSOR #81-003
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