Atlas FDA

PERIO CONTROL II

FDA 510(k) clearance K972642 · decided 1998-01-26

Clearance details

K-number
K972642
Device name
PERIO CONTROL II
Applicant
Estrad B.V.
Decision
Substantially Equivalent
Date received
1997-07-15
Decision date
1998-01-26
Days to decision
195 days
Clearance type
Traditional
Product code
EIK
Device class
1
Regulation number
872.4565
Medical specialty
Dental
Advisory committee
Dental
Location
Deer Field, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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ROOT CANAL ORGANIZER (K860817)Pacific Union Dental, Inc.1986-03-17
2020-1/2 TO 2220 VARIOUS DENTAL WAX & MODELLING CA (K851727)Artiberia1985-07-02

Recalls involving this device

No recalls on record reference this clearance.