Atlas FDA

ACETAL DENTAL/PREFORMED CLASP

FDA 510(k) clearance K955946 · decided 1995-12-11

Clearance details

K-number
K955946
Device name
ACETAL DENTAL/PREFORMED CLASP
Applicant
Pressing DI Monticelli Rag. Stefano
Decision
Substantially Equivalent
Date received
1995-10-27
Decision date
1995-12-11
Days to decision
45 days
Clearance type
Traditional
Product code
EHP
Device class
1
Regulation number
872.3285
Medical specialty
Dental
Advisory committee
Dental
Location
Cattilica, IT
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ACETAL (K022032)Inovativ, LLC2002-08-29
ACETAL DENTAL/PREFORMED CLASP (K983558)Dentamax, Inc.1999-01-07
DENTAL D (K974622)Micro Dental Laboratories1998-02-10
ACETAL DENTAL/PREFORMED CLASP (K954971)B & H Technical Services , Ltd.1995-12-11
INSTA-TOOTH SPLINT BAR WITH & WITHOUT TEETH (K854765)C&C Systems, Inc.1986-06-13
VACUDENT LUMIX 70 (K800575)Vacudent Sales Corp.1980-05-20
VACUDENT LUMIX 65 (K800574)Vacudent Sales Corp.1980-05-20

Recalls involving this device

No recalls on record reference this clearance.