FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

ULTRAPAK NEHA

K Number: K010070 · Decision Mar 15, 2001
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
35
Applicant Total
103
Review Days
66

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Basic Information

Device Name
ULTRAPAK NEHA
K Number
K010070
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ultradent Products, Inc.
Date Received
January 8, 2001
Decision Date
March 15, 2001
Product Code
MVL
Advisory Committee
Unknown
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
MVL Cord, Retraction

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