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

KLIP-LITE

K Number: K790984 · Decision Oct 22, 1979
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
22
Applicant Total
6
Review Days
150

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Basic Information

Device Name
KLIP-LITE
K Number
K790984
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4630
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Innovators, Inc.
Date Received
May 25, 1979
Decision Date
October 22, 1979
Product Code
EAZ
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
EAZ Light, Operating, Dental

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K Number Device Name
K921355 WINGMASTER
K921354 BLUNT TIP IRRIGATION NEEDLES
K921406 SILICONT BUR BLOCK
K844351 OPTI-LITE
K830042 E-Z JECTOR