FDA 510(k) FDA class 1 Unknown 🇺🇸 United States

GENERAL HYGIENE KIT

K Number: K954068 · Decision Nov 8, 1995
Classifications
1
FEI Numbers
148
Registration Numbers
148
Same Product Code
9
Applicant Total
4
Review Days
70

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Basic Information

Device Name
GENERAL HYGIENE KIT
K Number
K954068
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6050
Medical Specialty
Dental
Decision
Unknown
Statement or Summary
Statement
Applicant
Physician Industries, Inc.
Date Received
August 30, 1995
Decision Date
November 8, 1995
Product Code
KHR
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
KHR Absorber, Saliva, Paper

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Other Clearances by Physician Industries, Inc.

K Number Device Name
K040565 PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE
K033739 PHYSICIAN INDUSTRIES' DURAMETER SYRINGE
K960248 GENERAL PROCEDURE KIT