Atlas FDA

PRO-V

FDA 510(k) clearance K073263 · decided 2008-02-14

Clearance details

K-number
K073263
Device name
PRO-V
Applicant
Bisco, Inc.
Decision
Substantially Equivalent
Date received
2007-11-20
Decision date
2008-02-14
Days to decision
86 days
Clearance type
Traditional
Product code
EBG
Device class
2
Regulation number
872.3770
Medical specialty
Dental
Advisory committee
Dental
Location
Schaumburg, IL, US
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.

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TEMP MASTER, PMMA-based dental resin (K243951)Taiwan Dental Materials Co., Ltd.2025-02-21
PrimmaArt (K231859)Dentscare Ltda2024-11-26
Digital Temp (K242559)Sprintray, Inc.2024-11-26
Premium Teeth Resin (K240538)Formlabs Ohio, Inc.2024-07-19
Fixtemp® C&B 4:1 (K241226)Dreve Denatmid GmbH2024-05-31
dima Print Teeth & Temp (K233868)Kulzer, LLC2024-05-23
PMMA BLOCK (K223706)Huliang(Shanghai) Bio-Tech Co., Ltd.2023-05-12

Recalls involving this device

No recalls on record reference this clearance.